A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209530



Internal ID20776570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:110691663..110874873hg38UCSC Ensembl
chr4:111612819..111796029hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38183211
hg19183211
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6392597
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209530
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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