A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498574



Internal ID275564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73595554..73596639hg38UCSC Ensembl
chr13:74169691..74170776hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498574
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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