nsv4366041

Organism: Homo sapiens

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

Variant Calls:13
Validation:Not tested
Clinical Assertions: No
Region Size:510,797

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: 2839 SVs from 96 studies. See in: genome view

Remapped(Score: Good):21,994,497-22,505,293

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4366041	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nsv4366041	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	22,462,737	22,974,280

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15631779	copy number gain	10-0015-002	SNP array	Genotyping	17
nssv15672218	copy number gain	9-0017-001	SNP array	Genotyping	19
nssv15680570	copy number gain	214098	SNP array	Genotyping	20
nssv15684315	copy number gain	OCD1137-7286	SNP array	Genotyping	20
nssv15684869	copy number gain	OCD149-LF-1244	SNP array	Genotyping	19
nssv15686692	copy number gain	OCD160-0625-4932-3	SNP array	Genotyping	19
nssv15687609	copy number gain	OCD165-8961161	SNP array	Genotyping	15
nssv15688126	copy number gain	209355	SNP array	Genotyping	28
nssv15688248	copy number gain	210241	SNP array	Genotyping	23
nssv15689778	copy number gain	OCD1149-8961133	SNP array	Genotyping	18
nssv15690023	copy number gain	OCD1163-0625-7948-2	SNP array	Genotyping	22
nssv15696610	copy number gain	162332	SNP array	Genotyping	16
nssv15698218	copy number gain	80100	SNP array	Genotyping	25

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15631779	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15672218	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15680570	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15684315	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15684869	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15686692	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15687609	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15688126	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15688248	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15689778	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15690023	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15696610	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15698218	Remapped	Good	NC_000014.9:g.(?_2 1994497)_(22505293 _?)dup	GRCh38.p12	First Pass	NC_000014.9	Chr14	21,994,497	22,505,293
nssv15631779	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15672218	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15680570	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15684315	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15684869	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15686692	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15687609	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15688126	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15688248	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15689778	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15690023	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15696610	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280
nssv15698218	Submitted genomic		NC_000014.8:g.(?_2 2462737)_(22974280 _?)dup	GRCh37 (hg19)		NC_000014.8	Chr14	22,462,737	22,974,280

dbVar

Database of genomic structural variation

nsv4366041

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