A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155070



Internal ID22085575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19852340..20267598hg38UCSC Ensembl
Outerchr15:19830415..20283083hg38UCSC Ensembl
Innerchr15:20057593..20472851hg19UCSC Ensembl
Outerchr15:20035668..20488336hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38452669
hg19452669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4009750
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155070
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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