A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6694157



Internal ID10108313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:32708804..32709265hg38UCSC Ensembl
Outerchr6:32676581..32677042hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2731866, esv2731868, esv2731869, esv2731864
Supporting Variants
SamplesSSM037
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)essv6694157
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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