A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046963



Internal ID19136182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..21065709hg38UCSC Ensembl
Innerchr15:20590015..21271038hg19UCSC Ensembl
Innerchr15:18850029..19535697hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38680948
hg19681024
hg18685669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2237n100
Supporting Variantsnssv3539567
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, 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)nsv1046963
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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