A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262005



Internal ID20829045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32735345..32736091hg38UCSC Ensembl
chr3:32776837..32777583hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541759
Supporting Variants
Samples
Known GenesCNOT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262005
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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