A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460394



Internal ID238379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107260018..107263479hg38UCSC Ensembl
chr6:107581222..107584683hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383462
hg193462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987878
Samples
Known GenesPDSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460394
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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