A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18195279



Internal ID20762319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95454974..95535063hg38UCSC Ensembl
chr13:96107228..96187317hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3880090
hg1980090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477617
Supporting Variants
Samples
Known GenesCLDN10, CLDN10-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18195279
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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