A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18016369



Internal ID20583409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98608843..98631286hg38UCSC Ensembl
chr13:99261097..99283540hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3822444
hg1922444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487187
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18016369
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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