A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486283



Internal ID263652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102655881..102655933hg38UCSC Ensembl
chr8:103668109..103668161hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015807
Samples
Known GenesKLF10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486283
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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