A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6671076



Internal ID10086529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32505790..32544570hg38UCSC Ensembl
Outerchr6:32473567..32512347hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3838781
hg1938781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731844, esv2731846, esv2731839, esv2731842, esv2731835, esv2731837
Supporting Variants
SamplesSSM031
Known GenesHLA-DRB5
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)essv6671076
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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