A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262008



Internal ID20829048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32743045..32743610hg38UCSC Ensembl
chr3:32784537..32785102hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544331
Supporting Variants
Samples
Known GenesCNOT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262008
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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