A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544704



Internal ID21869059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43073969..43074025hg38UCSC Ensembl
chr3:43115461..43115517hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993855
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544704
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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