A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528657



Internal ID15109264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66524449..66558246hg38UCSC Ensembl
Innerchr14:66991167..67024964hg19UCSC Ensembl
Innerchr14:66060920..66094717hg18UCSC Ensembl
Innerchr14:66060920..66094717hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3833798
hg1933798
hg1833798
hg1733798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705291
Samples
Known GenesGPHN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528657
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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