A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043517



Internal ID18786048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101684138..101808429hg38UCSC Ensembl
Innerchr15:102224341..102348632hg19UCSC Ensembl
Innerchr15:100041864..100166155hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38124292
hg19124292
hg18124292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2683n100
Supporting Variantsnssv3718235
Samples
Known GenesOR4F6, TARSL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043517
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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