A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5494880



Internal ID272009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:33692949..33693029hg38UCSC Ensembl
chr13:34267086..34267166hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17686776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5494880
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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