A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17537317



Internal ID21861672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:171528862..171532243hg38UCSC Ensembl
chr2:172385372..172388753hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg383382
hg193382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987258
Supporting Variants
Samples
Known GenesCYBRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17537317
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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