A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047260



Internal ID18789791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:51964903..52045221hg38UCSC Ensembl
Innerchr15:52257100..52337418hg19UCSC Ensembl
Innerchr15:50044392..50124710hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3880319
hg1980319
hg1880319
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2595n100
Supporting Variantsnssv3552400
Samples
Known GenesLEO1, MAPK6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047260
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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