A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564745



Internal ID16352154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46317732..46404573hg38UCSC Ensembl
Innerchr14:46786935..46873776hg19UCSC Ensembl
Innerchr14:45856685..45943526hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3886842
hg1986842
hg1886842
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827682
Samples
Known GenesLINC00871
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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