A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280047



Internal ID20847087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130447009..130450556hg38UCSC Ensembl
chr9:133322396..133325943hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg383548
hg193548
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575440
Supporting Variants
Samples
Known GenesASS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280047
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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