A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011116



Internal ID19100333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75377944..75496021hg38UCSC Ensembl
Innerchr3:75427095..75545172hg19UCSC Ensembl
Innerchr3:75509785..75627862hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38118078
hg19118078
hg18118078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4774n100
Supporting Variantsnssv3733829, nssv3733077, nssv3602068, nssv3602084, nssv3602067, nssv3733824, nssv3602087, nssv3733822, nssv3733072, nssv3602090, nssv3733817, nssv3602062, nssv3733819, nssv3733826, nssv3602064, nssv3733820, nssv3602063, nssv3733075, nssv3602089, nssv3602076, nssv3733832, nssv3733818, nssv3733076, nssv3733071, nssv3602085, nssv3602088, nssv3602081, nssv3602086, nssv3733836, nssv3602082, nssv3602074, nssv3733830, nssv3602075, nssv3733833, nssv3733821, nssv3733835, nssv3602080, nssv3602065, nssv3733074, nssv3733823, nssv3602072, nssv3733070, nssv3602079, nssv3733831, nssv3733073, nssv3602060, nssv3602071, nssv3602083, nssv3733825, nssv3602066, nssv3602078, nssv3602069, nssv3733827, nssv3733816, nssv3602070, nssv3733834, nssv3602073, nssv3602077, nssv3733828, nssv3602061
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)nsv1011116
Frequency
Sample Size11257
Observed Gain0
Observed Loss60
Observed Complex0
Frequencyn/a


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