A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589417



Internal ID16030140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4046892..4062242hg38UCSC Ensembl
Innerchr3:4088576..4103926hg19UCSC Ensembl
Innerchr3:4063576..4078926hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3815351
hg1915351
hg1815351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8177n54
Supporting Variantsnssv958016, nssv958018, nssv958017
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589417
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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