A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213692



Internal ID20780732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:45646296..45676880hg38UCSC Ensembl
chr4:45648313..45678897hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3830585
hg1930585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378869
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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