A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6676498



Internal ID9747168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:31409859..31504963hg38UCSC Ensembl
Outerchr6:31377636..31472740hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3895105
hg1995105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731812, esv2731822
Supporting Variants
SamplesSSM032
Known GenesHCG26, HCP5, MICA, MICB
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)essv6676498
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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