A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506011



Internal ID282769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:58513954..58525165hg38UCSC Ensembl
chr13:59088088..59099299hg19UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3811212
hg1911212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506011
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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