A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527004



Internal ID15454297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42922904..43086586hg38UCSC Ensembl
Innerchr14:43392107..43555789hg19UCSC Ensembl
Innerchr14:42461857..42625539hg18UCSC Ensembl
Innerchr14:42461857..42625539hg17UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38163683
hg19163683
hg18163683
hg17163683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703379
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527004
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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