A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396300



Internal ID21053853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:256401..406800hg38UCSC Ensembl
chr6:256401..406800hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38150400
hg19150400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6038n223
Supporting Variantsnssv18236606
Samples
Known GenesDUSP22, IRF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396300
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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