A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040277



Internal ID19129496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101684138..101738603hg38UCSC Ensembl
Innerchr15:102224341..102278806hg19UCSC Ensembl
Innerchr15:100041864..100096329hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3854466
hg1954466
hg1854466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2682n100
Supporting Variantsnssv3555395, nssv3555396
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)nsv1040277
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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