A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521915



Internal ID15449208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24446177..24523413hg38UCSC Ensembl
Innerchr14:24915383..24992619hg19UCSC Ensembl
Innerchr14:23985223..24062459hg18UCSC Ensembl
Innerchr14:23985223..24062459hg17UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3877237
hg1977237
hg1877237
hg1777237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv128n21
Supporting Variantsnssv694686
Samples
Known GenesCMA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521915
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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