A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048142



Internal ID19137361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31799278..32127868hg38UCSC Ensembl
Innerchr15:32091481..32420069hg19UCSC Ensembl
Innerchr15:29878773..30207361hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38328591
hg19328589
hg18328589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2537n100
Supporting Variantsnssv3547714
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)nsv1048142
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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