A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491335



Internal ID268576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77341000..77369265hg38UCSC Ensembl
chr8:78253236..78281501hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3828266
hg1928266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012287
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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