A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457513



Internal ID235556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177829324..177844412hg38UCSC Ensembl
chr5:177256325..177271413hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3815089
hg1915089
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457513
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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