A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590258



Internal ID16377667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:50330728..50343591hg38UCSC Ensembl
Innerchr3:50368159..50381022hg19UCSC Ensembl
Innerchr3:50343163..50356026hg18UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3812864
hg1912864
hg1812864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv963023
Samples
Known GenesRASSF1, ZMYND10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590258
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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