A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2716792



Internal ID9951081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:10915552..10916174hg38UCSC Ensembl
Outerchr18:10915550..10916172hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38623
hg19623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6852410, essv6772860
SamplesSSM065, SSM086
Known GenesPIEZO2
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)esv2716792
Frequency
Sample Size96
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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