A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532837



Internal ID308750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6657107..6657420hg38UCSC Ensembl
chr19:6657118..6657431hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17720951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532837
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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