A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042589



Internal ID19131808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..19936692hg38UCSC Ensembl
Innerchr15:20016316..20141945hg19UCSC Ensembl
Innerchr15:18276329..18401959hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38125630
hg19125630
hg18125631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2170n100
Supporting Variantsnssv3714547
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)nsv1042589
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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