A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5454691



Internal ID232788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73369860..73383682hg38UCSC Ensembl
chr6:74079583..74093405hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3813823
hg1913823
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16984145
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5454691
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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