A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979056



Internal ID12632876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38503878..38681970hg38UCSC Ensembl
Innerchr9:38503875..38681967hg19UCSC Ensembl
Innerchr9:38493875..38671967hg18UCSC Ensembl
Innerchr9:38493875..38671967hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38178093
hg19178093
hg18178093
hg17178093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34705
Supporting Variants
SamplesNA12872
Known GenesANKRD18A, FAM201A, FAM95C
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979056
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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