A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497883



Internal ID274898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90823659..90858573hg38UCSC Ensembl
chr13:91475913..91510827hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3834915
hg1934915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497883
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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