A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465606



Internal ID243465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137710669..137726929hg38UCSC Ensembl
chr6:138031806..138048066hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3816261
hg1916261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970143
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465606
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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