A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383974



Internal ID21041527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102609242..102641695hg38UCSC Ensembl
chr4:103530399..103562852hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3832454
hg1932454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209444
Samples
Known GenesMANBA, NFKB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383974
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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