A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565762



Internal ID16006485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:99603617..99604555hg38UCSC Ensembl
Innerchr14:100069954..100070892hg19UCSC Ensembl
Innerchr14:99139707..99140645hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg38939
hg19939
hg18939
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833045
Samples
Known GenesCCDC85C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565762
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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