A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549638



Internal ID21873993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50786917..50797646hg38UCSC Ensembl
chr3:50824348..50835077hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3810730
hg1910730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993729
Supporting Variants
Samples
Known GenesDOCK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549638
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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