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dbVar

Database of genomic structural variation

nsv6297659

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:131

Description:nsv5462909 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: 123 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):155,194,161-155,194,291

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6297659	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	155,194,161	155,194,291
nsv6297659	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	156,115,313	156,115,443

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17668287	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17668287	Remapped	Perfect	NC_000004.12:g.155 194161_155194291du p	GRCh38.p12	First Pass	NC_000004.12	Chr4	155,194,161	155,194,291
nssv17668287	Submitted genomic		NC_000004.11:g.156 115313_156115443du p	GRCh37 (hg19)		NC_000004.11	Chr4	156,115,313	156,115,443

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)
nssv17668287	0.011	72	6320

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