A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1010587



Internal ID7074538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22493401..22571432hg38UCSC Ensembl
Innerchr15:23301664..23379695hg19UCSC Ensembl
Innerchr15:20853105..20931136hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3878032
hg1978032
hg1878032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586463
SamplesHuRef
Known GenesHERC2P2
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1010587
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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