Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv5613696

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

Submitted genomic196,335,389-196,335,389

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5613696	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	196,335,389	196,335,389
nsv5613696	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	196,062,260	196,062,260

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17122747	insertion	SAMN00001229	Sequencing	Sequence alignment	1,149

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17122747	Submitted genomic		NC_000003.12:g.196 335389_196335390in s71	GRCh38 (hg38)		NC_000003.12	Chr3	196,335,389	196,335,389
nssv17122747	Remapped	Perfect	NC_000003.11:g.196 062260_196062261in s71	GRCh37.p13	First Pass	NC_000003.11	Chr3	196,062,260	196,062,260

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.

You are here: NCBI