A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291335



Internal ID20500553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:52532802..52532867hg38UCSC Ensembl
chr3:52566818..52566883hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741817
Supporting Variants
Samples
Known GenesNT5DC2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291335
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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