A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589420



Internal ID16030143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046892..4242079hg38UCSC Ensembl
Innerchr3:4088576..4283763hg19UCSC Ensembl
Innerchr3:4063576..4258763hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38195188
hg19195188
hg18195188
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8174n54
Supporting Variantsnssv1152453
Samples1782681313_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589420
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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