A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933426



Internal ID22708738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77061300..77064242hg38UCSC Ensembl
chr15:77353642..77356584hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg382943
hg192943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389607
Samples
Known GenesTSPAN3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933426
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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