A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18194555



Internal ID20761595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:45350039..45350618hg38UCSC Ensembl
chr13:45924174..45924753hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38580
hg19580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6478555
Supporting Variants
Samples
Known GenesTPT1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18194555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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