A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5461331



Internal ID239285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63008791..63146668hg38UCSC Ensembl
chr6:63718696..63856573hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38137878
hg19137878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984346
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5461331
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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