A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215966



Internal ID20783006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:164110349..164124092hg38UCSC Ensembl
chr5:163537355..163551098hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3813744
hg1913744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215966
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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