A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526083



Internal ID21850441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:21932658..21932998hg38UCSC Ensembl
chr2:22155530..22155870hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5988145
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526083
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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