A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455833



Internal ID233905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:616408..867927hg38UCSC Ensembl
chr6:616408..867927hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38251520
hg19251520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979821
Samples
Known GenesEXOC2, HUS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455833
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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