A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218263



Internal ID20785303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14447326..14447973hg38UCSC Ensembl
chr11:14468872..14469519hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38648
hg19648
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595368
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218263
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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