A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290927



Internal ID20500145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158827901..158827960hg38UCSC Ensembl
chr3:158545690..158545749hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730727
Supporting Variants
Samples
Known GenesMFSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290927
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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