A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5531011



Internal ID306975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19371036..19371140hg38UCSC Ensembl
chr19:19481845..19481949hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722102
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5531011
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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