A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6832937



Internal ID10232938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:126971507..126971841hg38UCSC Ensembl
Outerchr2:127729083..127729417hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2720725
Supporting Variants
SamplesSSM082
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)essv6832937
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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