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dbVar

Database of genomic structural variation

nsv6115769

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:6,237

Description:nsv5415998 from Byrska-Bishop et. al 2021. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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: 357 SVs from 47 studies. See in: genome view

Remapped(Score: Perfect):11,935,080-11,941,316

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6115769	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	11,935,080	11,941,316
nsv6115769	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	11,953,199	11,959,435

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17960761	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17960761	Remapped	Perfect	NC_000023.11:g.119 35080_11941316del	GRCh38.p12	First Pass	NC_000023.11	ChrX	11,935,080	11,941,316
nssv17960761	Submitted genomic		NC_000023.10:g.119 53199_11959435del	GRCh37 (hg19)		NC_000023.10	ChrX	11,953,199	11,959,435

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17960761	0.45	2881	6404

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