A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6887126



Internal ID9935388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:167402679..167402871hg38UCSC Ensembl
Outerchr6:167816167..167816359hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2733238, esv2733230
Supporting Variants
SamplesSSM096
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)essv6887126
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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