A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394483



Internal ID21052036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125654819..125744471hg38UCSC Ensembl
chr4:126575974..126665626hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg3889653
hg1989653
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394483
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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