A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141318



Internal ID340513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85290290..85290971hg38UCSC Ensembl
chr6:86000008..86000689hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg38682
hg19682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984331
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141318
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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