A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186401



Internal ID20753441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76914815..76919311hg38UCSC Ensembl
chr13:77488949..77493445hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg384497
hg194497
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489326
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186401
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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