A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521114



Internal ID297415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38261378..38262306hg38UCSC Ensembl
chr19:38752018..38752946hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17723245
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521114
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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