A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935675



Internal ID22711020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62111905..62117025hg38UCSC Ensembl
chr15:62404104..62409224hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg385121
hg195121
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935675
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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