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dbVar

Database of genomic structural variation

nsv5534903

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: 79 SVs from 14 studies. See in: genome view

Submitted genomic63,674,290-63,674,290

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5534903	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	63,674,290	63,674,290
nsv5534903	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	64,384,191	64,384,191

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16986055	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16986055	Submitted genomic		NC_000006.12:g.636 74290_63674291ins1 22	GRCh38 (hg38)		NC_000006.12	Chr6	63,674,290	63,674,290
nssv16986055	Remapped	Perfect	NC_000006.11:g.643 84191_64384192ins1 22	GRCh37.p13	First Pass	NC_000006.11	Chr6	64,384,191	64,384,191

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)
nssv16986055	0.998	5563	5574

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