A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491090



Internal ID268335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:34615014..34615631hg38UCSC Ensembl
chr8:34472532..34473149hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011353
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491090
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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