A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5988332



Internal ID21897675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24041355..24045335hg38UCSC Ensembl
chr2:24264225..24268205hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383981
hg193981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17519218
Samples
Known GenesC2orf44
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5988332
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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