A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5534971



Internal ID310690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77036103..77036103hg38UCSC Ensembl
chr8:77948339..77948339hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5534971
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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