A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054792



Internal ID18797323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84192647..84557218hg38UCSC Ensembl
Innerchr15:84861399..85100449hg19UCSC Ensembl
Innerchr15:82652403..82901453hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38364572
hg19239051
hg18249051
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2638n100
Supporting Variantsnssv3718128
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)nsv1054792
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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