A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17547382



Internal ID21871737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:192828588..192828649hg38UCSC Ensembl
chr3:192546377..192546438hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5992468
Supporting Variants
Samples
Known GenesMB21D2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17547382
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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