A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223898



Internal ID20790938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33647110..33648214hg38UCSC Ensembl
chr11:33668656..33669760hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594049
Supporting Variants
Samples
Known GenesKIAA1549L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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