A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461920



Internal ID239863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109319888..109319962hg38UCSC Ensembl
chr6:109641091..109641165hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16986372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461920
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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