A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262834



Internal ID20829874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49761354..49763139hg38UCSC Ensembl
chr3:49798787..49800572hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg381786
hg191786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545352
Supporting Variants
Samples
Known GenesIP6K1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262834
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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