A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217807



Internal ID20784847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43383728..43383886hg38UCSC Ensembl
chr11:43405278..43405436hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578848
Supporting Variants
Samples
Known GenesTTC17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217807
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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