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dbVar

Database of genomic structural variation

nsv5609018

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 genomic196,811,213-196,811,213

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5609018	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	196,811,213	196,811,213
nsv5609018	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	196,538,084	196,538,084

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17130122	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17130122	Submitted genomic		NC_000003.12:g.196 811213_196811214in s529	GRCh38 (hg38)		NC_000003.12	Chr3	196,811,213	196,811,213
nssv17130122	Remapped	Perfect	NC_000003.11:g.196 538084_196538085in s529	GRCh37.p13	First Pass	NC_000003.11	Chr3	196,538,084	196,538,084

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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