A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280480



Internal ID20847520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:31937650..32149852hg38UCSC Ensembl
chr9:31937648..32149850hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38212203
hg19212203
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559717
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280480
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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