A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180782



Internal ID20747822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87740080..87794473hg38UCSC Ensembl
chr13:88392335..88446728hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3854394
hg1954394
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6481406
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180782
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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