A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461534



Internal ID239483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:174813378..174813688hg38UCSC Ensembl
chr5:174240381..174240691hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976768
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461534
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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