A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209544



Internal ID20776584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112220901..112237400hg38UCSC Ensembl
chr4:113142057..113158556hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3816500
hg1916500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6390605
Supporting Variants
Samples
Known GenesAP1AR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209544
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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