A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18009483



Internal ID20576523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50381831..50385349hg38UCSC Ensembl
chr13:50955967..50959485hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg383519
hg193519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495469
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18009483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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