A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890189



Internal ID22665215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:108562514..108562570hg38UCSC Ensembl
chr5:107898215..107898271hg19UCSC Ensembl
Cytoband5q21.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17424299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890189
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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