A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589807



Internal ID16377216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:15803854..15807823hg38UCSC Ensembl
Innerchr3:15845361..15849330hg19UCSC Ensembl
Innerchr3:15820365..15824334hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg383970
hg193970
hg183970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8240n54
Supporting Variantsnssv959658
Samples
Known GenesANKRD28
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589807
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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