A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586929



Internal ID6711625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92959922..92960364hg38UCSC Ensembl
Innerchr9:95722204..95722646hg19UCSC Ensembl
Innerchr9:94762025..94762467hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38443
hg19443
hg18443
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv989428
Supporting Variants
SamplesHuRef
Known GenesFGD3
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586929
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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