A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213505



Internal ID20780545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:34585864..34611785hg38UCSC Ensembl
chr4:34587486..34613407hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3825922
hg1925922
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363748
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213505
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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