A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523456



Internal ID15450749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81670496..81706040hg38UCSC Ensembl
Innerchr14:82136840..82172384hg19UCSC Ensembl
Innerchr14:81206593..81242137hg18UCSC Ensembl
Innerchr14:81206593..81242137hg17UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3835545
hg1935545
hg1835545
hg1735545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv139n21
Supporting Variantsnssv699214
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523456
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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