A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141766



Internal ID340963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67585025..67585083hg38UCSC Ensembl
chr8:68497260..68497318hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17011841
Samples
Known GenesCPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141766
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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