A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262351



Internal ID20829391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81723683..81726304hg38UCSC Ensembl
chr3:81772834..81775455hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg382622
hg192622
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544219
Supporting Variants
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262351
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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