A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943589



Internal ID22719039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58310994..58311288hg38UCSC Ensembl
chr15:58603193..58603487hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943589
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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