A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521246



Internal ID297542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33158123..33158207hg38UCSC Ensembl
chr19:33649029..33649113hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17722861
Samples
Known GenesWDR88
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521246
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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