A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048879



Internal ID19138098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31719274..32137531hg38UCSC Ensembl
Innerchr15:32011477..32429732hg19UCSC Ensembl
Innerchr15:29798769..30217024hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38418258
hg19418256
hg18418256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2536n100
Supporting Variantsnssv3547672
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)nsv1048879
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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