A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038883



Internal ID19128102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381394..22070662hg38UCSC Ensembl
Innerchr15:20586647..22358613hg19UCSC Ensembl
Innerchr15:18846661..19859977hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381689269
hg191771967
hg181013317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3538701
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, 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)nsv1038883
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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