A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5995575



Internal ID21904918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165251606..165251923hg38UCSC Ensembl
chr4:166172758..166173075hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17543788
Samples
Known GenesKLHL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5995575
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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