A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5530534



Internal ID306514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17589870..17589934hg38UCSC Ensembl
chr19:17700679..17700743hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721958
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5530534
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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