A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231082



Internal ID20798122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128570556..128571129hg38UCSC Ensembl
chr11:128440451..128441024hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593621
Supporting Variants
Samples
Known GenesETS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231082
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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