A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213556



Internal ID20780596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3846139..3950459hg38UCSC Ensembl
chr4:3847866..3952186hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38104321
hg19104321
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363260
Supporting Variants
Samples
Known GenesFAM86EP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213556
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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