A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262014



Internal ID20829054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32777727..32778170hg38UCSC Ensembl
chr3:32819219..32819662hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262014
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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