A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6938916



Internal ID9701903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:29741852..29812722hg38UCSC Ensembl
Outerchr6:29709629..29780499hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3870871
hg1970871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731768, esv2731767
Supporting Variants
SamplesSSM022
Known GenesHCG4, HLA-F-AS1, IFITM4P, LOC554223
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)essv6938916
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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