A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042439



Internal ID19131658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31681269..32220007hg38UCSC Ensembl
Innerchr15:31973472..32512208hg19UCSC Ensembl
Innerchr15:29760764..30299500hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38538739
hg19538737
hg18538737
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2535n100
Supporting Variantsnssv3547659, nssv3547658
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)nsv1042439
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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