A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527977



Internal ID15455270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:53453460..53472402hg38UCSC Ensembl
Innerchr14:53920178..53939120hg19UCSC Ensembl
Innerchr14:52989928..53008870hg18UCSC Ensembl
Innerchr14:52989928..53008870hg17UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3818943
hg1918943
hg1818943
hg1718943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704492
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527977
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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