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dbVar

Database of genomic structural variation

nsv5536924

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:1

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: 106 SVs from 23 studies. See in: genome view

Submitted genomic51,686,722-51,686,722

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5536924	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	51,686,722	51,686,722
nsv5536924	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	51,978,919	51,978,919

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17702706	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17702706	Submitted genomic		NC_000015.10:g.516 86722_51686723ins1 37	GRCh38 (hg38)		NC_000015.10	Chr15	51,686,722	51,686,722
nssv17702706	Remapped	Perfect	NC_000015.9:g.5197 8919_51978920ins13 7	GRCh37.p13	First Pass	NC_000015.9	Chr15	51,978,919	51,978,919

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)
nssv17702706	0.04	254	6350

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