A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929237



Internal ID22704487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75115693..75115751hg38UCSC Ensembl
chr15:75408034..75408092hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929237
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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