A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590380



Internal ID16377789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:59161214..59267021hg38UCSC Ensembl
Innerchr3:59146940..59252747hg19UCSC Ensembl
Innerchr3:59121980..59227787hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38105808
hg19105808
hg18105808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963381
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590380
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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