A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565992



Internal ID16353401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103520468..103523318hg38UCSC Ensembl
Innerchr14:103986805..103989655hg19UCSC Ensembl
Innerchr14:103056558..103059408hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg382851
hg192851
hg182851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3940n54
Supporting Variantsnssv834343
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565992
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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