A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701288



Internal ID15437940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132848903..132883495hg38UCSC Ensembl
Innerchr7:132533663..132568255hg19UCSC Ensembl
Innerchr7:132184203..132218795hg18UCSC Ensembl
Innerchr7:131990918..132025510hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3834593
hg1934593
hg1834593
hg1734593
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525206
Supporting Variants
Samples
Known GenesCHCHD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701288
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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