A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6589858



Internal ID20962929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122854400..122855196hg38UCSC Ensembl
chr11:122725108..122725904hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38797
hg19797
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221940
Samples
Known GenesCRTAM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6589858
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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