A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155198



Internal ID22085703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77702240..77715743hg38UCSC Ensembl
Outerchr15:77697620..77727959hg38UCSC Ensembl
Innerchr15:77994582..78008085hg19UCSC Ensembl
Outerchr15:77989962..78020301hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3830340
hg1930340
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4012129
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155198
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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