A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280854



Internal ID20847894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70397486..70398495hg38UCSC Ensembl
chr9:73012402..73013411hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg381010
hg191010
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568574
Supporting Variants
Samples
Known GenesKLF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280854
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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