A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051560



Internal ID18794091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:99296897..99584278hg38UCSC Ensembl
Innerchr15:99837102..100124483hg19UCSC Ensembl
Innerchr15:97654625..97942006hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38287382
hg19287382
hg18287382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555293
Samples
Known GenesLRRC28, MEF2A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051560
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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