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dbVar

Database of genomic structural variation

nsv5548407

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: 163 SVs from 33 studies. See in: genome view

Submitted genomic42,353,893-42,353,893

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5548407	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	42,353,893	42,353,893
nsv5548407	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	42,211,411	42,211,411

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17010769	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17010769	Submitted genomic		NC_000008.11:g.423 53893_42353894ins1 54	GRCh38 (hg38)		NC_000008.11	Chr8	42,353,893	42,353,893
nssv17010769	Remapped	Perfect	NC_000008.10:g.422 11411_42211412ins1 54	GRCh37.p13	First Pass	NC_000008.10	Chr8	42,211,411	42,211,411

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)
nssv17010769	0.016	101	6330

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