A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054979



Internal ID19144198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31722139..32220007hg38UCSC Ensembl
Innerchr15:32014342..32512208hg19UCSC Ensembl
Innerchr15:29801634..30299500hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38497869
hg19497867
hg18497867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2535n100
Supporting Variantsnssv3721603
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054979
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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