A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv828824



Internal ID15776094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:69572972..69574091hg38UCSC Ensembl
Innerchr14:70039689..70040808hg19UCSC Ensembl
Innerchr14:69109442..69110561hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg381120
hg191120
hg181120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565006
Supporting Variants
Samples
Known GenesCCDC177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv828824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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