A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527051



Internal ID15454344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3063897..3075426hg38UCSC Ensembl
Innerchr16:3113898..3125427hg19UCSC Ensembl
Innerchr16:3053899..3065428hg18UCSC Ensembl
Innerchr16:3053899..3065428hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3811530
hg1911530
hg1811530
hg1711530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv159n21
Supporting Variantsnssv703427
Samples
Known GenesIL32
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527051
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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