A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262502



Internal ID20471720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29317424..29317735hg38UCSC Ensembl
chr13:29891561..29891872hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741754
Supporting Variants
Samples
Known GenesMTUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262502
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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