A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890941



Internal ID22665972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53757714..53763712hg38UCSC Ensembl
chr5:53053544..53059542hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg385999
hg195999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890941
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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