A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590681



Internal ID16378090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75403949..75500011hg38UCSC Ensembl
Innerchr3:75453100..75549162hg19UCSC Ensembl
Innerchr3:75535790..75631852hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3896063
hg1996063
hg1896063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8384n54
Supporting Variantsnssv965710, nssv965707, nssv965712, nssv965708, nssv965711, nssv965713, nssv965705, nssv965706, nssv965709
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590681
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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