A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16291168



Internal ID20500386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36308716..36308772hg38UCSC Ensembl
chr13:36882853..36882909hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740563
Supporting Variants
Samples
Known GenesSPG20
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16291168
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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