A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17553600



Internal ID21877955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171998580..171998698hg38UCSC Ensembl
chr3:171716370..171716488hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5991982
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17553600
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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