A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590168



Internal ID20963239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:14391336..14393550hg38UCSC Ensembl
chr11:14412882..14415096hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg382215
hg192215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230081
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590168
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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