A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998190



Internal ID19157727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75483268hg38UCSC Ensembl
Innerchr3:75427095..75532419hg19UCSC Ensembl
Innerchr3:75509785..75615109hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38105325
hg19105325
hg18105325
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3733055, nssv3733056, nssv3733054, nssv3733051, nssv3733049, nssv3733050, nssv3733053, nssv3602037, nssv3602035, nssv3602034, nssv3733052, nssv3733057, nssv3602036
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998190
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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