A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564062



Internal ID16351471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24446177..24523413hg38UCSC Ensembl
Innerchr14:24915383..24992619hg19UCSC Ensembl
Innerchr14:23985223..24062459hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3877237
hg1977237
hg1877237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv824392
Samples
Known GenesCMA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564062
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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