A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038082



Internal ID19127301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20884473hg38UCSC Ensembl
Innerchr15:20284054..21089802hg19UCSC Ensembl
Innerchr15:18544068..19354467hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38805673
hg19805749
hg18810400
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2182n100
Supporting Variantsnssv3536554
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038082
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