A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6887722



Internal ID9666727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:31328404..31336903hg38UCSC Ensembl
Outerchr6:31296181..31304680hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731820, esv2731814, esv2731812
Supporting Variants
SamplesSSM012
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)essv6887722
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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