A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465656



Internal ID243515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14980086..15134257hg38UCSC Ensembl
chr5:14980195..15134366hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38154172
hg19154172
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962703
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465656
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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