A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041582



Internal ID19130801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:92336614..92367076hg38UCSC Ensembl
Innerchr15:92879844..92910306hg19UCSC Ensembl
Innerchr15:90680848..90711310hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3830463
hg1930463
hg1830463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555229
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041582
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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