A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233324



Internal ID20800364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:38260634..38378585hg38UCSC Ensembl
chr11:38282184..38400135hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38117952
hg19117952
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594426
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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