A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152259



Internal ID15879420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75379524..75519068hg38UCSC Ensembl
Innerchr3:75428675..75568219hg19UCSC Ensembl
Innerchr3:75511365..75650909hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38139545
hg19139545
hg18139545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590659
Supporting Variants
SamplesHGDP01362
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152259
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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