A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213677



Internal ID20780717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:44809043..44830118hg38UCSC Ensembl
chr4:44811060..44832135hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3821076
hg1921076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6383210
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213677
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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