A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593993



Internal ID20967064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3790914..3791439hg38UCSC Ensembl
chr11:3812144..3812669hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222328
Samples
Known GenesNUP98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593993
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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