A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259111



Internal ID20468299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101704484..101705296hg38UCSC Ensembl
chr13:102356834..102357646hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745458
Supporting Variants
Samples
Known GenesITGBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259111
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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