A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988115



Internal ID21897458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23668828..23668965hg38UCSC Ensembl
chr2:23891698..23891835hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527806
Samples
Known GenesKLHL29
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988115
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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