A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221853



Internal ID20788893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62731751..62732647hg38UCSC Ensembl
chr11:62499223..62500119hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38897
hg19897
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579185
Supporting Variants
Samples
Known GenesTTC9C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221853
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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