A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6965305



Internal ID9722898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71296846..71296942hg38UCSC Ensembl
Outerchr10:73056603..73056699hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738262, esv2738251
Supporting Variants
SamplesSSM027
Known GenesUNC5B
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6965305
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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