A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488061



Internal ID265382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61819836..61823343hg38UCSC Ensembl
chr8:62732395..62735902hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg383508
hg193508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488061
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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