A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6711587



Internal ID9649199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:122696739..122710346hg38UCSC Ensembl
Outerchr12:123181286..123194893hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3813608
hg1913608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2746500
Supporting Variants
SamplesSSM006
Known GenesHCAR2
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)essv6711587
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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