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

dbVar

Database of genomic structural variation

nsv5836066

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:1,100

Publication(s):Almarri et al. 2020

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: 95 SVs from 24 studies. See in: genome view

Submitted genomic51,901,537-51,902,636

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5836066	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	51,901,537	51,902,636
nsv5836066	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	51,935,553	51,936,652

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
nssv17493229	copy number variation	Sequencing	Sequence alignment	0
nssv17493230	copy number variation	Sequencing	Sequence alignment	2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17493229	Submitted genomic		GRCh38 (hg38)		NC_000003.12	Chr3	51,901,537	51,902,636
nssv17493230	Submitted genomic		GRCh38 (hg38)		NC_000003.12	Chr3	51,901,537	51,902,636
nssv17493229	Remapped	Perfect	GRCh37.p13	First Pass	NC_000003.11	Chr3	51,935,553	51,936,652
nssv17493230	Remapped	Perfect	GRCh37.p13	First Pass	NC_000003.11	Chr3	51,935,553	51,936,652

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