A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6918833



Internal ID10029227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32709642..32709997hg38UCSC Ensembl
Outerchr6:32677419..32677774hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731866, esv2731868, esv2731864
Supporting Variants
SamplesSSM017
Known Genes
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)essv6918833
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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