A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17533441



Internal ID21857797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:85451375..85451442hg38UCSC Ensembl
chr2:85678498..85678565hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990182
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17533441
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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