A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16274736



Internal ID20483954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45377948..45378028hg38UCSC Ensembl
chr13:45952083..45952163hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4740686
Supporting Variants
Samples
Known GenesTPT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16274736
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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