A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3586216



Internal ID7057598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61518913..61665737hg38UCSC Ensembl
Innerchr9:44726751..44873575hg19UCSC Ensembl
Innerchr9:44666747..44813571hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38146825
hg19146825
hg18146825
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv988098
Supporting Variants
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3586216
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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