A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527905



Internal ID15455198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:83390603..83477976hg38UCSC Ensembl
Innerchr14:83856947..83944320hg19UCSC Ensembl
Innerchr14:82926700..83014073hg18UCSC Ensembl
Innerchr14:82926700..83014073hg17UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg3887374
hg1987374
hg1887374
hg1787374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704409
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527905
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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