A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383786



Internal ID21041339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:116780635..116785309hg38UCSC Ensembl
chr4:117701791..117706465hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg384675
hg194675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383786
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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