A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv832991



Internal ID15780261
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 StatusS
Merged Variantsnsv565736
Supporting Variants
Samples
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv832991
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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