A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3587131



Internal ID6711827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98747509..98748223hg38UCSC Ensembl
Innerchr9:101509791..101510505hg19UCSC Ensembl
Innerchr9:100549612..100550326hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38715
hg19715
hg18715
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989098
Supporting Variants
SamplesHuRef
Known GenesANKS6
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3587131
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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