A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590314



Internal ID20963385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112303027..112398617hg38UCSC Ensembl
chr11:112173750..112269340hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3895591
hg1995591
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590314
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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