A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589415



Internal ID16030138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046892..4058193hg38UCSC Ensembl
Innerchr3:4088576..4099877hg19UCSC Ensembl
Innerchr3:4063576..4074877hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3811302
hg1911302
hg1811302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8177n54
Supporting Variantsnssv958009
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589415
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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