A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045254



Internal ID19134473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20538504hg38UCSC Ensembl
Innerchr15:20216943..20743782hg19UCSC Ensembl
Innerchr15:18476957..19003796hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38526815
hg19526840
hg18526840
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2186n100
Supporting Variantsnssv3536952, nssv3536953
Samples
Known GenesCHEK2P2, GOLGA6L6, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045254
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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