A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482524



Internal ID259979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19817666..19818221hg38UCSC Ensembl
chr8:19675177..19675732hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009106
Samples
Known GenesINTS10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482524
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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