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dbVar

Database of genomic structural variation

nsv5543265

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:221

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: 136 SVs from 46 studies. See in: genome view

Submitted genomic28,781,368-28,781,588

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5543265	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	28,781,368	28,781,588
nsv5543265	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	29,177,356	29,177,576

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17728327	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17728327	Submitted genomic		NC_000022.11:g.287 81368_28781588ins6 26	GRCh38 (hg38)		NC_000022.11	Chr22	28,781,368	28,781,588
nssv17728327	Remapped	Perfect	NC_000022.10:g.291 77356_29177576ins6 26	GRCh37.p13	First Pass	NC_000022.10	Chr22	29,177,356	29,177,576

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)
nssv17728327	0.823	5274	6404

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