A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6918716



Internal ID9682436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:29870414..29999813hg38UCSC Ensembl
Outerchr6:29838191..29967590hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38129400
hg19129400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731775
Supporting Variants
SamplesSSM017
Known GenesHCG4B, HCG9, HLA-A, HLA-H
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)essv6918716
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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