A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942630



Internal ID22718071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58356691..58360400hg38UCSC Ensembl
chr15:58648890..58652599hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg383710
hg193710
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385867
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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