A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558548



Internal ID20931619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:117406126..117419893hg38UCSC Ensembl
chr4:118327282..118341049hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3813768
hg1913768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18264165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558548
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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