A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583974



Internal ID20957045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118665977..118667081hg38UCSC Ensembl
chr11:118536686..118537790hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236155
Samples
Known GenesTREH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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