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dbVar

Database of genomic structural variation

nsv6131202

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:4

Description:nsv5550263 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: 105 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):53,898,930-53,898,933

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6131202	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	53,898,930	53,898,933
nsv6131202	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	54,402,184	54,402,187

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17959412	insertion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17959412	Remapped	Perfect	NC_000019.10:g.538 98930_53898933ins?	GRCh38.p12	First Pass	NC_000019.10	Chr19	53,898,930	53,898,933
nssv17959412	Submitted genomic		NC_000019.9:g.5440 2184_54402187ins?	GRCh37 (hg19)		NC_000019.9	Chr19	54,402,184	54,402,187

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)
nssv17959412	0.061	383	6262

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