A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv159n21



Internal ID22766351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3063897..3075426hg38UCSC Ensembl
chr16:3113898..3125427hg19UCSC Ensembl
chr16:3053899..3065428hg18UCSC Ensembl
chr16:3053899..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 Variants
Supporting Variantsnsv527051, nsv525573
Samples
Known GenesIL32
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv159n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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