A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665312



Internal ID15401964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132883495..132935604hg38UCSC Ensembl
Innerchr7:132568255..132620364hg19UCSC Ensembl
Innerchr7:132218795..132270904hg18UCSC Ensembl
Innerchr7:132025510..132077619hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3852110
hg1952110
hg1852110
hg1752110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515919
Supporting Variants
Samples
Known GenesCHCHD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665312
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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