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dbVar

Database of genomic structural variation

nsv6123689

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:1

Description:nsv5538856 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: 131 SVs from 21 studies. See in: genome view

Remapped(Score: Perfect):118,212,773-118,212,773

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6123689	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	118,212,773	118,212,773
nsv6123689	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	118,533,936	118,533,936

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17961794	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17961794	Remapped	Perfect	NC_000006.12:g.118 212773_118212774in s?	GRCh38.p12	First Pass	NC_000006.12	Chr6	118,212,773	118,212,773
nssv17961794	Submitted genomic		NC_000006.11:g.118 533936_118533937in s?	GRCh37 (hg19)		NC_000006.11	Chr6	118,533,936	118,533,936

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)
nssv17961794	0.157	1003	6404

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