A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589782



Internal ID16377191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15797254..15804672hg38UCSC Ensembl
Innerchr3:15838761..15846179hg19UCSC Ensembl
Innerchr3:15813765..15821183hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg387419
hg197419
hg187419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8236n54
Supporting Variantsnssv959450, nssv959451
Samples
Known GenesANKRD28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589782
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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