A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499501



Internal ID276473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:74418771..74419177hg38UCSC Ensembl
chr13:74992908..74993314hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17691781
Samples
Known GenesLINC00381
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499501
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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