A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565754



Internal ID16006477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99603237..99616411hg38UCSC Ensembl
Innerchr14:100069574..100082748hg19UCSC Ensembl
Innerchr14:99139327..99152501hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3813175
hg1913175
hg1813175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3892n54
Supporting Variantsnssv833035
Samples
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565754
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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