A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495998



Internal ID273089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59096061..59096157hg38UCSC Ensembl
chr13:59670195..59670291hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688208
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495998
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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