A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572586



Internal ID16359995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:49855934..49858140hg38UCSC Ensembl
Innerchr16:49889845..49892051hg19UCSC Ensembl
Innerchr16:48447346..48449552hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg382207
hg192207
hg182207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5117n54
Supporting Variantsnssv857284
Samples
Known GenesZNF423
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572586
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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