A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7703n100



Internal ID22793790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112954828..113027616hg38UCSC Ensembl
chr9:115717108..115789896hg19UCSC Ensembl
chr9:114756929..114829717hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3872789
hg1972789
hg1872789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035654, nsv1040477, nsv1052547
Samples
Known GenesZNF883
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7703n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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