A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376390



Internal ID21033943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:133354101..133405900hg38UCSC Ensembl
chr4:134275256..134327055hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3851800
hg1951800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376390
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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