A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2722922



Internal ID10306558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63409729..63409897hg38UCSC Ensembl
Outerchr20:62041082..62041250hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6946059, essv6960887, essv6804182, essv6816244, essv6873886, essv6801227, essv6913595, essv6852711
SamplesSSM011, SSM073, SSM023, SSM026, SSM086, SSM072, SSM015, SSM077
Known GenesKCNQ2
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)esv2722922
Frequency
Sample Size96
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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