A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529151



Internal ID305186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:17409337..17409965hg38UCSC Ensembl
chr19:17520146..17520774hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17721943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529151
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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