A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564970



Internal ID16005693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:69533682..69573444hg38UCSC Ensembl
Innerchr14:70000399..70040161hg19UCSC Ensembl
Innerchr14:69070152..69109914hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3839763
hg1939763
hg1839763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828632
Samples
Known GenesCCDC177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564970
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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