A curated catalogue of human genomic structural variation




Variant Details

Variant: esv987865



Internal ID7075363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41231308..41237517hg38UCSC Ensembl
Innerchr17:39387560..39393769hg19UCSC Ensembl
Innerchr17:36641086..36647295hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg386210
hg196210
hg186210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586003
SamplesHuRef
Known GenesKRTAP9-3
MethodSNP array
AnalysisPooled samples.
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv987865
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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