A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590642



Internal ID16378051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75339010..75519068hg38UCSC Ensembl
Innerchr3:75388161..75568219hg19UCSC Ensembl
Innerchr3:75470851..75650909hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38180059
hg19180059
hg18180059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152258
SamplesHGDP00902
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590642
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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