A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459836



Internal ID237842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154953429..154955981hg38UCSC Ensembl
chr6:155274563..155277115hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382553
hg192553
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990095
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459836
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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