A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6922994



Internal ID9685532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:29397348..29418011hg38UCSC Ensembl
Outerchr6:29365125..29385788hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3820664
hg1920664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731763
Supporting Variants
SamplesSSM018
Known GenesOR12D2
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)essv6922994
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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