A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526651



Internal ID21851009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38883883..38883969hg38UCSC Ensembl
chr2:39111024..39111110hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989147
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526651
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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