A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6384239



Internal ID21041792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:163399122..163454988hg38UCSC Ensembl
chr4:164320274..164376140hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg3855867
hg1955867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6384239
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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