A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155184



Internal ID22085689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59420228..59649523hg38UCSC Ensembl
Outerchr15:59419492..59652284hg38UCSC Ensembl
Innerchr15:59712427..59941722hg19UCSC Ensembl
Outerchr15:59711691..59944483hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38232793
hg19232793
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011101
Samples
Known GenesFAM81A, GCNT3, GTF2A2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155184
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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