A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477010



Internal ID254607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85808800..85915222hg38UCSC Ensembl
chr8:86821029..86927451hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg38106423
hg19106423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17013426
Samples
Known GenesREXO1L2P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477010
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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