A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152260



Internal ID15853916
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
Samples1780854483_A
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152260
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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