A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6779868



Internal ID10185361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:64340960..64341254hg38UCSC Ensembl
Outerchr15:64633159..64633453hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2749781
Supporting Variants
SamplesSSM067
Known GenesCSNK1G1
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)essv6779868
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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