A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589789



Internal ID16377198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15802839..15804877hg38UCSC Ensembl
Innerchr3:15844346..15846384hg19UCSC Ensembl
Innerchr3:15819350..15821388hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg382039
hg192039
hg182039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8237n54
Supporting Variantsnssv959466, nssv959464, nssv959462, nssv959463, nssv959465
Samples
Known GenesANKRD28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589789
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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