A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527052



Internal ID15107659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:58487186..58508997hg38UCSC Ensembl
Innerchr16:58521090..58542901hg19UCSC Ensembl
Innerchr16:57078591..57100402hg18UCSC Ensembl
Innerchr16:57078591..57100402hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3821812
hg1921812
hg1821812
hg1721812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703428
Samples
Known GenesNDRG4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527052
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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