A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6968951



Internal ID9643146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:71296588..71297126hg38UCSC Ensembl
Outerchr10:73056345..73056883hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738251
Supporting Variants
SamplesSSM004
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)essv6968951
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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