A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590396



Internal ID16377805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60344625..60462257hg38UCSC Ensembl
Innerchr3:60330356..60447990hg19UCSC Ensembl
Innerchr3:60305396..60423030hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38117633
hg19117635
hg18117635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8342n54
Supporting Variantsnssv963403
Samples
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590396
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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