A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499699



Internal ID276661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:28652475..28652551hg38UCSC Ensembl
chr13:29226612..29226688hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499699
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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