A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696791



Internal ID15086757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:35672892..35726322hg38UCSC Ensembl
Innerchr7:35712502..35765932hg19UCSC Ensembl
Innerchr7:35679027..35732457hg18UCSC Ensembl
Innerchr7:35485742..35539172hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3853431
hg1953431
hg1853431
hg1753431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519322
Supporting Variants
Samples
Known GenesHERPUD2, LOC100506725
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696791
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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