A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506112



Internal ID282866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99577875..99580576hg38UCSC Ensembl
chr13:100230129..100232830hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg382702
hg192702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692598
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506112
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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