A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281203



Internal ID20490421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:72725456..72726156hg38UCSC Ensembl
chr13:73299594..73300294hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4735459
Supporting Variants
Samples
Known GenesMZT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281203
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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