A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279873



Internal ID20846913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125220291..125221150hg38UCSC Ensembl
chr9:127982570..127983429hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38860
hg19860
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565831
Supporting Variants
Samples
Known GenesRABEPK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279873
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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