A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038143



Internal ID19127362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20894299hg38UCSC Ensembl
Innerchr15:20262224..21099628hg19UCSC Ensembl
Innerchr15:18522238..19364287hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38837329
hg19837405
hg18842050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2182n100
Supporting Variantsnssv3715858
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)nsv1038143
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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