A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115543



Internal ID21298809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:13571286..13575490hg38UCSC Ensembl
Innerchr9:13571285..13575489hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg384205
hg194205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1220n145
Supporting Variantsnssv14090770, nssv14089577, nssv14089509, nssv14089483, nssv14089708, nssv14088427, nssv14090839, nssv14089648, nssv14088412, nssv14087914, nssv14090793, nssv14089764, nssv14089565, nssv14088155, nssv14087950, nssv14089755, nssv14088432, nssv14090773, nssv14088053, nssv14089475, nssv14089603, nssv14088072, nssv14089580, nssv14088819
Samplessample365, sample170, sample9, sample142, sample87, sample165, sample202, sample312, sample181, sample59, sample320, sample390, sample169, sample19, sample44, sample81, sample118, sample18, sample89, sample250, sample99, sample46, sample162, sample268
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115543
Frequency
Sample Size467
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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