A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5527952



Internal ID304031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:58353526..58355573hg38UCSC Ensembl
chr19:58864892..58866939hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382048
hg192048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17724447
Samples
Known GenesA1BG-AS1, ZNF497
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5527952
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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