A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282162



Internal ID20491380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79419083..79419154hg38UCSC Ensembl
chr13:79993218..79993289hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745932
Supporting Variants
Samples
Known GenesRBM26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282162
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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