A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563985



Internal ID336909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88501016..88501067hg38UCSC Ensembl
chr8:89513245..89513296hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17014864
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563985
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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