A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527406



Internal ID15454699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:49773811..49774621hg38UCSC Ensembl
Innerchr16:49807722..49808532hg19UCSC Ensembl
Innerchr16:48365223..48366033hg18UCSC Ensembl
Innerchr16:48365223..48366033hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38811
hg19811
hg18811
hg17811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703843
Samples
Known GenesZNF423
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527406
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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