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dbVar

Database of genomic structural variation

nsv5534325

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:459

Publication(s):Byrska-Bishop et al. 2022

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: 208 SVs from 37 studies. See in: genome view

Submitted genomic7,387,367-7,387,825

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5534325	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	7,387,367	7,387,825
nsv5534325	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	7,389,094	7,389,552

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16945441	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16945441	Submitted genomic		NC_000004.12:g.738 7367_7387825ins451	GRCh38 (hg38)		NC_000004.12	Chr4	7,387,367	7,387,825
nssv16945441	Remapped	Perfect	NC_000004.11:g.738 9094_7389552ins451	GRCh37.p13	First Pass	NC_000004.11	Chr4	7,389,094	7,389,552

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16945441	0.245	1547	6324

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