A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392597



Internal ID21050150
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 StatusM
Merged Variants
Supporting Variantsnssv18209530
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392597
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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