A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572589



Internal ID16359998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:49856114..49858729hg38UCSC Ensembl
Innerchr16:49890025..49892640hg19UCSC Ensembl
Innerchr16:48447526..48450141hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg382616
hg192616
hg182616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5117n54
Supporting Variantsnssv857287
Samples
Known GenesZNF423
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572589
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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