A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477035



Internal ID254630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11800911..11800989hg38UCSC Ensembl
chr8:11658420..11658498hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17008319
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477035
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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