A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565005



Internal ID16005728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:69572870..69574240hg38UCSC Ensembl
Innerchr14:70039587..70040957hg19UCSC Ensembl
Innerchr14:69109340..69110710hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg381371
hg191371
hg181371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3744n54
Supporting Variantsnssv828823
Samples
Known GenesCCDC177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565005
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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