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dbVar

Database of genomic structural variation

nsv5537432

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: 83 SVs from 24 studies. See in: genome view

Submitted genomic157,139,720-157,139,720

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5537432	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	157,139,720	157,139,720
nsv5537432	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	156,566,731	156,566,731

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16975927	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16975927	Submitted genomic		NC_000005.10:g.157 139720_157139721in s326	GRCh38 (hg38)		NC_000005.10	Chr5	157,139,720	157,139,720
nssv16975927	Remapped	Perfect	NC_000005.9:g.1565 66731_156566732ins 326	GRCh37.p13	First Pass	NC_000005.9	Chr5	156,566,731	156,566,731

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)
nssv16975927	0.107	647	6060

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