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dbVar

Database of genomic structural variation

nsv6074774

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Wu et al. 2021

Links to Other Resources

Overlapping Genes

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: 131 SVs from 30 studies. See in: genome view

Submitted genomic119,296,228-119,296,228

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6074774	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	119,296,228	119,296,228
nsv6074774	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	120,217,383	120,217,383

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17557534	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17557534	Submitted genomic		NC_000004.12:g.119 296228_119296229in s302	GRCh38 (hg38)		NC_000004.12	Chr4	119,296,228	119,296,228
nssv17557534	Remapped	Perfect	NC_000004.11:g.120 217383_120217384in s302	GRCh37.p13	First Pass	NC_000004.11	Chr4	120,217,383	120,217,383

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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