A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544807



Internal ID21869162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184099714..184103605hg38UCSC Ensembl
chr3:183817502..183821393hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg383892
hg193892
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992405
Supporting Variants
Samples
Known GenesHTR3E
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544807
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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