A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589785



Internal ID16377194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15797254..15804877hg38UCSC Ensembl
Innerchr3:15838761..15846384hg19UCSC Ensembl
Innerchr3:15813765..15821388hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg387624
hg197624
hg187624
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8236n54
Supporting Variantsnssv959456, nssv959454, nssv959455
Samples
Known GenesANKRD28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589785
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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