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dbVar

Database of genomic structural variation

nsv6129398

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:nsv5543998 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: 182 SVs from 31 studies. See in: genome view

Remapped(Score: Perfect):77,815,892-77,815,892

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6129398	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	77,815,892	77,815,892
nsv6129398	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	77,849,789	77,849,789

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17966543	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17966543	Remapped	Perfect	NC_000016.10:g.778 15892_77815893ins?	GRCh38.p12	First Pass	NC_000016.10	Chr16	77,815,892	77,815,892
nssv17966543	Submitted genomic		NC_000016.9:g.7784 9789_77849790ins?	GRCh37 (hg19)		NC_000016.9	Chr16	77,849,789	77,849,789

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)
nssv17966543	0.771	4744	6154

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