A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292675



Internal ID20501893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:29492085..29492139hg38UCSC Ensembl
chr13:30066222..30066276hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732158
Supporting Variants
Samples
Known GenesMTUS2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292675
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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