A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565736



Internal ID16006459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99589871..99604392hg38UCSC Ensembl
Innerchr14:100056208..100070729hg19UCSC Ensembl
Innerchr14:99125961..99140482hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3814522
hg1914522
hg1814522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3885n54
Supporting Variantsnssv832991
Samples
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565736
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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