A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211070



Internal ID20778110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134492601..134522800hg38UCSC Ensembl
chr4:135413756..135443955hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3830200
hg1930200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384968
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211070
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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