A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998631



Internal ID6734563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:71795372..71796041hg38UCSC Ensembl
Innerchr10:73555129..73555798hg19UCSC Ensembl
Innerchr10:73225135..73225804hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38670
hg19670
hg18670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586845
SamplesHuRef
Known GenesCDH23, MIR6797
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998631
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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