A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260147



Internal ID20469365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45042603..45042674hg38UCSC Ensembl
chr21:46462518..46462589hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4736501
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260147
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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