A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049846



Internal ID19139065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31648339..32285928hg38UCSC Ensembl
Innerchr15:31940542..32578129hg19UCSC Ensembl
Innerchr15:29727834..30365421hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38637590
hg19637588
hg18637588
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2535n100
Supporting Variantsnssv3547657
Samples
Known GenesCHRNA7, OTUD7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049846
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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