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dbVar

Database of genomic structural variation

nsv5623317

Organism: Homo sapiens

Study:nstd207 (Ebert 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):Ebert 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: 94 SVs from 26 studies. See in: genome view

Submitted genomic13,377,787-13,377,787

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5623317	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	13,377,787	13,377,787
nsv5623317	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	13,419,287	13,419,287

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17134848	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17134848	Submitted genomic		NC_000003.12:g.133 77787_13377788ins6 7	GRCh38 (hg38)		NC_000003.12	Chr3	13,377,787	13,377,787
nssv17134848	Remapped	Perfect	NC_000003.11:g.134 19287_13419288ins6 7	GRCh37.p13	First Pass	NC_000003.11	Chr3	13,419,287	13,419,287

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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