A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213903



Internal ID20780943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153011001..153053900hg38UCSC Ensembl
chr5:152390561..152433460hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3842900
hg1942900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403728
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213903
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00074


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