A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556463



Internal ID20929534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23424631..23427370hg38UCSC Ensembl
chr6:23424859..23427598hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382740
hg192740
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6092n223
Supporting Variantsnssv18270841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556463
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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