A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003073



Internal ID19092290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75496659hg38UCSC Ensembl
Innerchr3:75427095..75545810hg19UCSC Ensembl
Innerchr3:75509785..75628500hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38118716
hg19118716
hg18118716
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3733838, nssv3602094, nssv3602093, nssv3602100, nssv3602099, nssv3602104, nssv3733837, nssv3733839, nssv3602102, nssv3602091, nssv3733840, nssv3602098, nssv3602101, nssv3602096, nssv3602095, nssv3602103, nssv3602092, nssv3602097
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)nsv1003073
Frequency
Sample Size11257
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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