A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213696



Internal ID20780736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45780701..45806400hg38UCSC Ensembl
chr4:45782718..45808417hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3825700
hg1925700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385916
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00091


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