A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564954



Internal ID16005677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66577385..66658067hg38UCSC Ensembl
Innerchr14:67044103..67124785hg19UCSC Ensembl
Innerchr14:66113856..66194538hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3880683
hg1980683
hg1880683
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828619
Samples
Known GenesGPHN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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