A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269143



Internal ID20478361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58570588..58570640hg38UCSC Ensembl
chr3:58556315..58556367hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4737336
Supporting Variants
Samples
Known GenesFAM107A
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269143
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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