A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042493



Internal ID19131712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31696725..32151995hg38UCSC Ensembl
Innerchr15:31988928..32444196hg19UCSC Ensembl
Innerchr15:29776220..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38455271
hg19455269
hg18455269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2536n100
Supporting Variantsnssv3547667, nssv3547666, nssv3721590
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)nsv1042493
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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