A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523556



Internal ID15450849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16285977..16291205hg38UCSC Ensembl
Innerchr20:16266622..16271850hg19UCSC Ensembl
Innerchr20:16214622..16219850hg18UCSC Ensembl
Innerchr20:16214622..16219850hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg385229
hg195229
hg185229
hg175229
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699335
Samples
Known GenesKIF16B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523556
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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