A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521291



Internal ID15448584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81670496..81707997hg38UCSC Ensembl
Innerchr14:82136840..82174341hg19UCSC Ensembl
Innerchr14:81206593..81244094hg18UCSC Ensembl
Innerchr14:81206593..81244094hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3837502
hg1937502
hg1837502
hg1737502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv139n21
Supporting Variantsnssv697894
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521291
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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