A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279488



Internal ID20846528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109135479..109135969hg38UCSC Ensembl
chr9:111897759..111898249hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571135
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279488
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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