A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009834



Internal ID20576874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46145627..46145956hg38UCSC Ensembl
chr13:46719762..46720091hg19UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476810
Supporting Variants
Samples
Known GenesLCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.40155


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