A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17530011



Internal ID21854367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201198835..201211946hg38UCSC Ensembl
chr2:202063558..202076669hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3813112
hg1913112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5987167
Supporting Variants
Samples
Known GenesCASP10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17530011
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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