A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564952



Internal ID16352361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65792676..65821256hg38UCSC Ensembl
Innerchr14:66259394..66287974hg19UCSC Ensembl
Innerchr14:65329147..65357727hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3828581
hg1928581
hg1828581
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149498
SamplesHGDP00696
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564952
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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