A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2737566



Internal ID10321202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:127407919..127408192hg38UCSC Ensembl
Outerchr8:128420164..128420437hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6672204, essv6677255, essv6795425, essv6834402, essv6861699, essv6958248, essv6897233, essv6908308, essv6838080, essv6716206
SamplesSSM083, SSM071, SSM088, SSM026, SSM032, SSM031, SSM014, SSM082, SSM099, SSM043
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)esv2737566
Frequency
Sample Size96
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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