A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6759994



Internal ID9820590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:31410041..31504668hg38UCSC Ensembl
Outerchr6:31377818..31472445hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3894628
hg1994628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731812, esv2731822
Supporting Variants
SamplesSSM061
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)essv6759994
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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