A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466682



Internal ID244514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103309807..103437807hg38UCSC Ensembl
chr5:102645508..102773508hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38128001
hg19128001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16971784
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466682
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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