A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6862119



Internal ID9911595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131939202..131939329hg38UCSC Ensembl
Outerchr10:133752706..133752833hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2743588, esv2743584
Supporting Variants
SamplesSSM088
Known GenesPPP2R2D
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)essv6862119
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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