A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122824



Internal ID20689864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114985566..114993222hg38UCSC Ensembl
chr5:114321263..114328919hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg387657
hg197657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6406854
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122824
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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