A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6949484



Internal ID9635887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:29898262..29959006hg38UCSC Ensembl
Outerchr6:29866039..29926783hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3860745
hg1960745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731769
Supporting Variants
SamplesSSM001
Known GenesHCG4B, HLA-A
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)essv6949484
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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