A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141469



Internal ID340665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74511265..74803265hg38UCSC Ensembl
chr8:75423500..75715500hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38292001
hg19292001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012172
Samples
Known GenesFLJ39080, MIR2052, MIR5681A, MIR5681B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141469
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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