A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6869656



Internal ID9919488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:30098249..30100906hg38UCSC Ensembl
Outerchr6:30066026..30068683hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg382658
hg192658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731780, esv2731777
Supporting Variants
SamplesSSM090
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)essv6869656
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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