A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035183



Internal ID19124402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100415526..100548027hg38UCSC Ensembl
Innerchr15:100955731..101088232hg19UCSC Ensembl
Innerchr15:98773254..98905755hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38132502
hg19132502
hg18132502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718222
Samples
Known GenesCERS3, PRKXP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035183
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