A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384131



Internal ID21041684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163353685..163374681hg38UCSC Ensembl
chr4:164274837..164295833hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3820997
hg1920997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213758
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384131
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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