A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226568



Internal ID20793608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111789326..111789824hg38UCSC Ensembl
chr11:111660050..111660548hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38499
hg19499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584833
Supporting Variants
Samples
Known GenesALG9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226568
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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