A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460400



Internal ID238385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:80000..1240000hg38UCSC Ensembl
chr6:80000..1240235hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381160001
hg191160236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16977921
Samples
Known GenesDUSP22, EXOC2, HUS1B, IRF4, LOC285768
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460400
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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