A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17519218



Internal ID21843577
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 StatusS
Merged Variantsnsv5988332
Supporting Variants
Samples
Known GenesC2orf44
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17519218
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer