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dbVar

Database of genomic structural variation

nsv6130017

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:36

Description:nsv5539280 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: 189 SVs from 36 studies. See in: genome view

Remapped(Score: Perfect):82,794,362-82,794,397

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6130017	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	82,794,362	82,794,397
nsv6130017	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	82,827,967	82,828,002

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17957635	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17957635	Remapped	Perfect	NC_000016.10:g.827 94362_82794397ins?	GRCh38.p12	First Pass	NC_000016.10	Chr16	82,794,362	82,794,397
nssv17957635	Submitted genomic		NC_000016.9:g.8282 7967_82828002ins?	GRCh37 (hg19)		NC_000016.9	Chr16	82,827,967	82,828,002

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)
nssv17957635	0.16	1023	6404

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