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dbVar

Database of genomic structural variation

nsv5549716

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: 97 SVs from 32 studies. See in: genome view

Submitted genomic55,687,190-55,687,190

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5549716	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	55,687,190	55,687,190
nsv5549716	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	55,721,102	55,721,102

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17705983	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17705983	Submitted genomic		NC_000016.10:g.556 87190_55687191ins1 10	GRCh38 (hg38)		NC_000016.10	Chr16	55,687,190	55,687,190
nssv17705983	Remapped	Perfect	NC_000016.9:g.5572 1102_55721103ins11 0	GRCh37.p13	First Pass	NC_000016.9	Chr16	55,721,102	55,721,102

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)
nssv17705983	0.988	6325	6402

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