A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460161



Internal ID238155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132754696..132762314hg38UCSC Ensembl
chr6:133075835..133083453hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg387619
hg197619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16970093
Samples
Known GenesVNN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460161
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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