A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528943



Internal ID15456236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:59143635..59147671hg38UCSC Ensembl
Innerchr16:59177539..59181575hg19UCSC Ensembl
Innerchr16:57735040..57739076hg18UCSC Ensembl
Innerchr16:57735040..57739076hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384037
hg194037
hg184037
hg174037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705634
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528943
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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