A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930148



Internal ID22705410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65805555..65811313hg38UCSC Ensembl
chr15:66097893..66103651hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385759
hg195759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17388575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930148
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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