A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5457718



Internal ID235757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165610114..165610189hg38UCSC Ensembl
chr5:165037119..165037194hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16975375
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5457718
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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