A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053626



Internal ID19142845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..20078801hg38UCSC Ensembl
Innerchr15:20016316..20284054hg19UCSC Ensembl
Innerchr15:18276329..18544068hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38267739
hg19267739
hg18267740
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2172n100
Supporting Variantsnssv3534423
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)nsv1053626
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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