A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6894625



Internal ID9941958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:10425729..10441235hg38UCSC Ensembl
Outerchr12:10578328..10593834hg19UCSC Ensembl
Cytoband12p13.2
Allele length
AssemblyAllele length
hg3815507
hg1915507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2745535
Supporting Variants
SamplesSSM098
Known GenesKLRC2
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)essv6894625
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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