A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5524561



Internal ID300763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44606649..44610217hg38UCSC Ensembl
chr19:45109966..45113535hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg383569
hg193570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv252n206
Supporting Variantsnssv17725246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5524561
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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