nsv4383158

Organism: Homo sapiens

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

Variant Calls:25
Validation:Not tested
Clinical Assertions: No
Region Size:41,009

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: 412 SVs from 70 studies. See in: genome view

Remapped(Score: Perfect):44,963,166-45,004,174

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4383158	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nsv4383158	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	44,965,183	45,006,191

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15616401	copy number gain	1-0823-003	SNP array	Genotyping	20
nssv15629860	copy number gain	1-0595-001	SNP array	Genotyping	31
nssv15629951	copy number gain	1-0595-004	SNP array	Genotyping	25
nssv15630560	copy number gain	1-0595-005	SNP array	Genotyping	21
nssv15632342	copy number gain	10-0002-003	SNP array	Genotyping	22
nssv15635619	copy number gain	13-0031-001	SNP array	Genotyping	18
nssv15640978	copy number gain	14-0319-002	SNP array	Genotyping	16
nssv15647421	copy number gain	2-1244-002	SNP array	Genotyping	22
nssv15648447	copy number gain	2-1294-003	SNP array	Genotyping	21
nssv15652337	copy number gain	2-1502-002	SNP array	Genotyping	22
nssv15652352	copy number gain	2-1502-003	SNP array	Genotyping	17
nssv15653759	copy number gain	2-1629-003	SNP array	Genotyping	16
nssv15653875	copy number gain	2-1598-003	SNP array	Genotyping	18
nssv15654399	copy number gain	2-1629-002	SNP array	Genotyping	18
nssv15657391	copy number gain	3-0490-000	SNP array	Genotyping	24
nssv15674677	copy number gain	222704	SNP array	Genotyping	20
nssv15675343	copy number gain	232813S	SNP array	Genotyping	27
nssv15676719	copy number gain	167696	SNP array	Genotyping	15
nssv15677086	copy number gain	218109	SNP array	Genotyping	21
nssv15681425	copy number gain	OCD103-1585	SNP array	Genotyping	20
nssv15684636	copy number gain	OCD151-RH-1295	SNP array	Genotyping	21
nssv15689028	copy number gain	228236	SNP array	Genotyping	21
nssv15689277	copy number gain	OCD10-S_896171	SNP array	Genotyping	23
nssv15689321	copy number gain	OCD10-S_896173	SNP array	Genotyping	23
nssv15692929	copy number gain	OCD77-896703	SNP array	Genotyping	27

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15616401	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15629860	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15629951	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15630560	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15632342	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15635619	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15640978	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15647421	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15648447	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15652337	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15652352	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15653759	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15653875	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15654399	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15657391	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15674677	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15675343	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15676719	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15677086	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15681425	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15684636	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15689028	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15689277	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15689321	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15692929	Remapped	Perfect	NC_000004.12:g.(?_ 44963166)_(4500417 4_?)dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	44,963,166	45,004,174
nssv15616401	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15629860	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15629951	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15630560	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15632342	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15635619	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15640978	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15647421	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15648447	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15652337	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15652352	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15653759	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15653875	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15654399	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15657391	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15674677	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15675343	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15676719	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15677086	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15681425	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15684636	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15689028	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15689277	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15689321	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191
nssv15692929	Submitted genomic		NC_000004.11:g.(?_ 44965183)_(4500619 1_?)dup	GRCh37 (hg19)		NC_000004.11	Chr4	44,965,183	45,006,191

dbVar

Database of genomic structural variation

nsv4383158

Links to Other Resources

Genome View

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