A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499052



Internal ID276032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42750485..42752776hg38UCSC Ensembl
chr13:43324621..43326912hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg382292
hg192292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17687237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499052
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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