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

dbVar

Database of genomic structural variation

nsv5570790

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:58

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: 111 SVs from 28 studies. See in: genome view

Submitted genomic133,446,570-133,446,627

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5570790	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	133,446,570	133,446,627
nsv5570790	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	133,165,414	133,165,471

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17128598	deletion	HG03371	Sequencing	Sequence alignment	2,852

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17128598	Submitted genomic		NC_000003.12:g.133 446570_133446627de lT	GRCh38 (hg38)		NC_000003.12	Chr3	133,446,570	133,446,627
nssv17128598	Remapped	Perfect	NC_000003.11:g.133 165414_133165471de lT	GRCh37.p13	First Pass	NC_000003.11	Chr3	133,165,414	133,165,471

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