A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016433



Internal ID20583473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99896963..99903800hg38UCSC Ensembl
chr13:100549217..100556054hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg386838
hg196838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6491480
Supporting Variants
Samples
Known GenesCLYBL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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