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dbVar

Database of genomic structural variation

nsv5622990

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Ebert et al. 2021

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

Submitted genomic196,811,226-196,811,226

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5622990	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	196,811,226	196,811,226
nsv5622990	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	196,538,097	196,538,097

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17126546	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17126546	Submitted genomic		NC_000003.12:g.196 811226_196811227in s4317	GRCh38 (hg38)		NC_000003.12	Chr3	196,811,226	196,811,226
nssv17126546	Remapped	Perfect	NC_000003.11:g.196 538097_196538098in s4317	GRCh37.p13	First Pass	NC_000003.11	Chr3	196,538,097	196,538,097

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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