A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6938784



Internal ID9642011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:10420504..10436044hg38UCSC Ensembl
Outerchr12:10573103..10588643hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3815541
hg1915541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745535
Supporting Variants
SamplesSSM003
Known GenesKLRC2, KLRC3
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)essv6938784
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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