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dbVar

Database of genomic structural variation

nsv6130326

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:43

Description:nsv5552331 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: 345 SVs from 32 studies. See in: genome view

Remapped(Score: Perfect):68,956,406-68,956,448

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6130326	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	68,956,406	68,956,448
nsv6130326	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000018.9	Chr18	66,623,643	66,623,685

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17958699	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17958699	Remapped	Perfect	NC_000018.10:g.689 56406_68956448ins?	GRCh38.p12	First Pass	NC_000018.10	Chr18	68,956,406	68,956,448
nssv17958699	Submitted genomic		NC_000018.9:g.6662 3643_66623685ins?	GRCh37 (hg19)		NC_000018.9	Chr18	66,623,643	66,623,685

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)
nssv17958699	0.156	941	6050

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