A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465059



Internal ID242929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177582677..177582759hg38UCSC Ensembl
chr5:177009678..177009760hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16976816
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465059
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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