A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490854



Internal ID268103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65616977..65617064hg38UCSC Ensembl
chr8:66529212..66529299hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013676
Samples
Known GenesARMC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490854
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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