A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221088



Internal ID20788128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31470135..31473345hg38UCSC Ensembl
chr11:31491682..31494892hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383211
hg193211
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575850
Supporting Variants
Samples
Known GenesIMMP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221088
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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