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dbVar

Database of genomic structural variation

nsv6129425

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:68

Description:nsv5534678 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: 195 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):84,916,173-84,916,240

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6129425	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000015.10	Chr15	84,916,173	84,916,240
nsv6129425	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000015.9	Chr15	85,459,404	85,459,471

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17966131	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17966131	Remapped	Perfect	NC_000015.10:g.849 16173_84916240ins?	GRCh38.p12	First Pass	NC_000015.10	Chr15	84,916,173	84,916,240
nssv17966131	Submitted genomic		NC_000015.9:g.8545 9404_85459471ins?	GRCh37 (hg19)		NC_000015.9	Chr15	85,459,404	85,459,471

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)
nssv17966131	0.262	1646	6274

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