A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2742676



Internal ID10296792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:16037119..16060477hg38UCSC Ensembl
Outerchr1:16363614..16386972hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3823359
hg1923359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9e201
Supporting Variantsessv6902531
SamplesSSM013
Known GenesCLCNKB, FAM131C
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)esv2742676
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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