A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041308



Internal ID19130527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70146633..70178938hg38UCSC Ensembl
Innerchr15:70438972..70471277hg19UCSC Ensembl
Innerchr15:68226026..68258331hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3832306
hg1932306
hg1832306
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2617n100
Supporting Variantsnssv3553670, nssv3553669
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041308
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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