A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6778137



Internal ID9837119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:31224604..31530772hg38UCSC Ensembl
Outerchr6:31192381..31498549hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38306169
hg19306169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731812
Supporting Variants
SamplesSSM067
Known GenesATP6V1G2-DDX39B, DDX39B, HCG26, HCP5, HLA-B, HLA-C, MCCD1, MICA, MICB, MIR6891
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)essv6778137
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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