A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465429



Internal ID243291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177953324..177980500hg38UCSC Ensembl
chr5:177380325..177407501hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3827177
hg1927177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv411n206
Supporting Variantsnssv16977688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465429
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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