A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214492



Internal ID20781532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:135784801..135802100hg38UCSC Ensembl
chr5:135120490..135137789hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3817300
hg1917300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6402547
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214492
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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