A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049114



Internal ID19138333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..19989473hg38UCSC Ensembl
Innerchr15:20016316..20194726hg19UCSC Ensembl
Innerchr15:18276329..18454740hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38178411
hg19178411
hg18178412
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2171n100
Supporting Variantsnssv3534418
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)nsv1049114
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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