A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573587



Internal ID16014310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88502831..88534082hg38UCSC Ensembl
Innerchr16:88569239..88600490hg19UCSC Ensembl
Innerchr16:87096740..87127991hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg3831252
hg1931252
hg1831252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5294n54
Supporting Variantsnssv862559
Samples
Known GenesZFPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573587
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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