A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048203



Internal ID19137422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19811063..19936028hg38UCSC Ensembl
Innerchr15:20016316..20141281hg19UCSC Ensembl
Innerchr15:18276329..18401295hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38124966
hg19124966
hg18124967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2170n100
Supporting Variantsnssv3534405
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048203
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