A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209545



Internal ID20776585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:11236501..11239800hg38UCSC Ensembl
chr4:11238125..11241424hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374801
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209545
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00095


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