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dbVar

Database of genomic structural variation

nsv5607028

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: 347 SVs from 53 studies. See in: genome view

Submitted genomic196,334,825-196,334,825

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5607028	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	196,334,825	196,334,825
nsv5607028	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	196,061,696	196,061,696

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17127518	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17127518	Submitted genomic		NC_000003.12:g.196 334825_196334826in s426	GRCh38 (hg38)		NC_000003.12	Chr3	196,334,825	196,334,825
nssv17127518	Remapped	Perfect	NC_000003.11:g.196 061696_196061697in s426	GRCh37.p13	First Pass	NC_000003.11	Chr3	196,061,696	196,061,696

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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