A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039388



Internal ID19128607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31799278..32128298hg38UCSC Ensembl
Innerchr15:32091481..32420499hg19UCSC Ensembl
Innerchr15:29878773..30207791hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38329021
hg19329019
hg18329019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2537n100
Supporting Variantsnssv3547715
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)nsv1039388
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer