A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583197



Internal ID20956268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107574651..107575637hg38UCSC Ensembl
chr11:107445377..107446363hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38987
hg19987
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583197
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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