A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996246



Internal ID21905589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165258286..165258411hg38UCSC Ensembl
chr4:166179438..166179563hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555291
Samples
Known GenesKLHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996246
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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