A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6574826



Internal ID20947897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:196714..448068hg38UCSC Ensembl
chr6:196714..448068hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38251355
hg19251355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18270137
Samples
Known GenesDUSP22, IRF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6574826
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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