A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6870399



Internal ID10266842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:77087072..77087254hg38UCSC Ensembl
Outerchr9:79701988..79702170hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg38183
hg19183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2738608, esv2738606
Supporting Variants
SamplesSSM090
Known Genes
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)essv6870399
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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