A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556042



Internal ID21880397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180514203..180514256hg38UCSC Ensembl
chr3:180231991..180232044hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992171
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556042
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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