A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5456496



Internal ID234559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:25282877..25282951hg38UCSC Ensembl
chr6:25283105..25283179hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980860
Samples
Known GenesLRRC16A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5456496
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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