A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280149



Internal ID20847189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135640062..135640478hg38UCSC Ensembl
chr9:138531908..138532324hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280149
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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