A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3554674



Internal ID18506269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82652403..82891471hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg18239069
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052911
Supporting Variants
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3554674
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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