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dbVar

Database of genomic structural variation

nsv5543464

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:35

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: 87 SVs from 21 studies. See in: genome view

Submitted genomic45,130,301-45,130,335

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5543464	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	45,130,301	45,130,335
nsv5543464	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	45,171,793	45,171,827

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16933694	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16933694	Submitted genomic		NC_000003.12:g.451 30301_45130335ins3 28	GRCh38 (hg38)		NC_000003.12	Chr3	45,130,301	45,130,335
nssv16933694	Remapped	Perfect	NC_000003.11:g.451 71793_45171827ins3 28	GRCh37.p13	First Pass	NC_000003.11	Chr3	45,171,793	45,171,827

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)
nssv16933694	0.002	16	6404

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