nsv4380121

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:56
Validation:Not tested
Clinical Assertions: No
Region Size:44,550

Publication(s):Zarrei et al. 2019

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 2109 SVs from 106 studies. See in: genome view

Remapped(Score: Perfect):29,873,244-29,917,793

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4380121	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nsv4380121	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	29,841,021	29,885,570

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15616161	copy number loss	1-0144-003	SNP array	Genotyping	20
nssv15618825	copy number loss	1-0889-003	SNP array	Genotyping	18
nssv15619087	copy number loss	1-0181-001	SNP array	Genotyping	15
nssv15620452	copy number loss	1-0935-003	SNP array	Genotyping	16
nssv15622419	copy number loss	1-1032-003	SNP array	Genotyping	19
nssv15622981	copy number loss	1-0236-003	SNP array	Genotyping	29
nssv15625512	copy number loss	1-0414-005	SNP array	Genotyping	14
nssv15628219	copy number loss	1-0488-003	SNP array	Genotyping	12
nssv15633200	copy number loss	11-0012-003	SNP array	Genotyping	22
nssv15635467	copy number loss	12-4453-001	SNP array	Genotyping	16
nssv15637318	copy number loss	13-0078-004	SNP array	Genotyping	20
nssv15638071	copy number loss	14-0063-003	SNP array	Genotyping	21
nssv15639457	copy number loss	14-0187-003	SNP array	Genotyping	21
nssv15640581	copy number loss	14-0344-001	SNP array	Genotyping	24
nssv15641131	copy number loss	14-0384-001	SNP array	Genotyping	28
nssv15642312	copy number loss	14-0385-001	SNP array	Genotyping	23
nssv15646153	copy number loss	16-1023-003	SNP array	Genotyping	26
nssv15646988	copy number loss	2-1213-001	SNP array	Genotyping	25
nssv15652341	copy number loss	2-1502-002	SNP array	Genotyping	22
nssv15660509	copy number loss	5-0003-004	SNP array	Genotyping	16
nssv15660829	copy number loss	4-0034-004	SNP array	Genotyping	21
nssv15661651	copy number loss	4-0030-002	SNP array	Genotyping	16
nssv15662506	copy number loss	5-0050-003	SNP array	Genotyping	17
nssv15662521	copy number loss	5-0050-004	SNP array	Genotyping	17
nssv15662804	copy number loss	5-0138-003	SNP array	Genotyping	26
nssv15667045	copy number loss	7-0149-003	SNP array	Genotyping	20
nssv15668069	copy number loss	7-0165-003	SNP array	Genotyping	24
nssv15668321	copy number loss	7-0189-003	SNP array	Genotyping	19
nssv15669274	copy number loss	7-0169-003	SNP array	Genotyping	14
nssv15674541	copy number loss	9-0045-002	SNP array	Genotyping	22
nssv15679332	copy number loss	218119	SNP array	Genotyping	29
nssv15681484	copy number loss	OCD107-1633	SNP array	Genotyping	17
nssv15681827	copy number loss	OCD108-1636	SNP array	Genotyping	16
nssv15684175	copy number loss	OCD1111-896063	SNP array	Genotyping	17
nssv15684305	copy number loss	OCD1135-5884	SNP array	Genotyping	18
nssv15685388	copy number loss	OCD118-S_1713	SNP array	Genotyping	18
nssv15686757	copy number loss	OCD26-S_896512	SNP array	Genotyping	19
nssv15686904	copy number loss	OCD37-S_0625-0201-1	SNP array	Genotyping	20
nssv15687088	copy number loss	OCD31-S_896573	SNP array	Genotyping	20
nssv15687121	copy number loss	OCD32-S_896581	SNP array	Genotyping	31
nssv15690321	copy number loss	OCD141-0625-7921-2	SNP array	Genotyping	26
nssv15690891	copy number loss	OCD171-BS-363_1771	SNP array	Genotyping	15
nssv15691457	copy number loss	OCD42-S_0625-2765-3	SNP array	Genotyping	27
nssv15691647	copy number loss	OCD74-RM-249	SNP array	Genotyping	18
nssv15691925	copy number loss	OCD82-896793	SNP array	Genotyping	25
nssv15692365	copy number loss	OCD6-S_896121	SNP array	Genotyping	21
nssv15692406	copy number loss	OCD6-S_896123	SNP array	Genotyping	23
nssv15692776	copy number loss	OCD72-896553	SNP array	Genotyping	17
nssv15693161	copy number loss	OCD86-896851	SNP array	Genotyping	29
nssv15693188	copy number loss	OCD87-896883	SNP array	Genotyping	19
nssv15693427	copy number loss	OCD7-S_896131	SNP array	Genotyping	27
nssv15694171	copy number loss	OCD81-896772	SNP array	Genotyping	18
nssv15695713	copy number loss	OCD99-1550	SNP array	Genotyping	31
nssv15697722	copy number loss	175285	SNP array	Genotyping	18
nssv15697846	copy number loss	194735	SNP array	Genotyping	21
nssv15702157	copy number loss	154658	SNP array	Genotyping	22

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15616161	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15618825	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15619087	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15620452	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15622419	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15622981	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15625512	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15628219	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15633200	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15635467	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15637318	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15638071	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15639457	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15640581	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15641131	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15642312	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15646153	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15646988	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15652341	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15660509	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15660829	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15661651	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15662506	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15662521	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15662804	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15667045	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15668069	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15668321	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15669274	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15674541	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15679332	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15681484	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15681827	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15684175	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15684305	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15685388	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15686757	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15686904	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15687088	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15687121	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15690321	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15690891	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15691457	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15691647	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15691925	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15692365	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15692406	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15692776	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15693161	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15693188	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15693427	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15694171	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15695713	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15697722	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15697846	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15702157	Remapped	Perfect	NC_000006.12:g.(?_ 29873244)_(2991779 3_?)del	GRCh38.p12	First Pass	NC_000006.12	Chr6	29,873,244	29,917,793
nssv15616161	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15618825	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15619087	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15620452	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15622419	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15622981	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15625512	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15628219	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15633200	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15635467	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15637318	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15638071	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15639457	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15640581	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15641131	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15642312	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15646153	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15646988	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15652341	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15660509	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15660829	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15661651	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15662506	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15662521	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15662804	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15667045	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15668069	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15668321	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15669274	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15674541	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15679332	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15681484	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15681827	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15684175	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15684305	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15685388	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15686757	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15686904	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15687088	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15687121	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15690321	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15690891	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15691457	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570
nssv15691647	Submitted genomic		NC_000006.11:g.(?_ 29841021)_(2988557 0_?)del	GRCh37 (hg19)		NC_000006.11	Chr6	29,841,021	29,885,570

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dbVar

Database of genomic structural variation

nsv4380121

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant