A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038859



Internal ID18781390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101684138..101805184hg38UCSC Ensembl
Innerchr15:102224341..102345387hg19UCSC Ensembl
Innerchr15:100041864..100162910hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38121047
hg19121047
hg18121047
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2683n100
Supporting Variantsnssv3718234
Samples
Known GenesTARSL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038859
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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