A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525849



Internal ID15453142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:21580280..21586908hg38UCSC Ensembl
Innerchr14:22048414..22055032hg19UCSC Ensembl
Innerchr14:21118254..21124872hg18UCSC Ensembl
Innerchr14:21118254..21124872hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg386629
hg196619
hg186619
hg176619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702043
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525849
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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