A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900523



Internal ID22675666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154611233..154614374hg38UCSC Ensembl
chr5:153990793..153993934hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg383142
hg193142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17426610
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900523
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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