A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516238



Internal ID15443531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:64860570..64891858hg38UCSC Ensembl
Innerchr14:65327288..65358576hg19UCSC Ensembl
Innerchr14:64397041..64428329hg18UCSC Ensembl
Innerchr14:64397041..64428329hg17UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3831289
hg1931289
hg1831289
hg1731289
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv666992, nssv692960
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516238
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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