A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18280403



Internal ID20847443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26870631..26871505hg38UCSC Ensembl
chr9:26870629..26871503hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38875
hg19875
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565222
Supporting Variants
Samples
Known GenesCAAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18280403
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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