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dbVar

Database of genomic structural variation

nsv6625508

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:3
Validation:Not tested
Clinical Assertions: No
Region Size:206,069

Publication(s):Zarrei et al. 2023

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: 1584 SVs from 93 studies. See in: genome view

Remapped(Score: Perfect):6,897,463-7,103,531

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6625508	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	6,897,463	7,103,531
nsv6625508	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	6,897,474	7,103,542

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18323098	duplication	OSC1460	SNP array	Probe signal intensity	7
nssv18324386	duplication	OSC1717	SNP array	Probe signal intensity	11
nssv18326135	duplication	OSC0208	SNP array	Probe signal intensity	8

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18323098	Remapped	Perfect	NC_000019.10:g.(?_ 6897463)_(7103531_ ?)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	6,897,463	7,103,531
nssv18324386	Remapped	Perfect	NC_000019.10:g.(?_ 6897463)_(7103531_ ?)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	6,897,463	7,103,531
nssv18326135	Remapped	Perfect	NC_000019.10:g.(?_ 6897463)_(7103531_ ?)dup	GRCh38.p12	First Pass	NC_000019.10	Chr19	6,897,463	7,103,531
nssv18323098	Submitted genomic		NC_000019.9:g.(?_6 897474)_(7103542_? )dup	GRCh37 (hg19)		NC_000019.9	Chr19	6,897,474	7,103,542
nssv18324386	Submitted genomic		NC_000019.9:g.(?_6 897474)_(7103542_? )dup	GRCh37 (hg19)		NC_000019.9	Chr19	6,897,474	7,103,542
nssv18326135	Submitted genomic		NC_000019.9:g.(?_6 897474)_(7103542_? )dup	GRCh37 (hg19)		NC_000019.9	Chr19	6,897,474	7,103,542

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

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