A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527284



Internal ID15454577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:59311543..59314926hg38UCSC Ensembl
Innerchr14:59778261..59781644hg19UCSC Ensembl
Innerchr14:58848014..58851397hg18UCSC Ensembl
Innerchr14:58848014..58851397hg17UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg383384
hg193384
hg183384
hg173384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703696
Samples
Known GenesDAAM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527284
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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