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dbVar

Database of genomic structural variation

nsv6126671

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:42

Description:nsv5546737 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: 149 SVs from 21 studies. See in: genome view

Remapped(Score: Perfect):125,098,606-125,098,647

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6126671	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	125,098,606	125,098,647
nsv6126671	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000010.10	Chr10	126,787,175	126,787,216

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17657892	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17657892	Remapped	Perfect	NC_000010.11:g.125 098606_125098647in s?	GRCh38.p12	First Pass	NC_000010.11	Chr10	125,098,606	125,098,647
nssv17657892	Submitted genomic		NC_000010.10:g.126 787175_126787216in s?	GRCh37 (hg19)		NC_000010.10	Chr10	126,787,175	126,787,216

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)
nssv17657892	0.474	3013	6360

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