A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589241



Internal ID16029964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:40338..143598hg38UCSC Ensembl
Innerchr3:82010..185281hg19UCSC Ensembl
Innerchr3:57010..160281hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38103261
hg19103272
hg18103272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8142n54
Supporting Variantsnssv1152225
SamplesHGDP00183
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589241
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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