A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214300



Internal ID20781340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:86018201..86062700hg38UCSC Ensembl
chr5:85314019..85358518hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3844500
hg1944500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398097
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00024


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