A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697298



Internal ID15433950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155274676..155287024hg38UCSC Ensembl
Innerchr7:155066386..155078734hg19UCSC Ensembl
Innerchr7:154697319..154709667hg18UCSC Ensembl
Innerchr7:154504034..154516382hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3812349
hg1912349
hg1812349
hg1712349
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519304
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697298
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer