A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534890



Internal ID21859245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:205793035..205815186hg38UCSC Ensembl
chr2:206657759..206679910hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3822152
hg1922152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987354
Supporting Variants
Samples
Known GenesNRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534890
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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