A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528691



Internal ID15455984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:63602088..63631837hg38UCSC Ensembl
Innerchr14:64068806..64098555hg19UCSC Ensembl
Innerchr14:63138559..63168308hg18UCSC Ensembl
Innerchr14:63138559..63168308hg17UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3829750
hg1929750
hg1829750
hg1729750
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705334
Samples
Known GenesWDR89
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528691
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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