A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261348



Internal ID20828388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31026140..31027157hg38UCSC Ensembl
chr3:31067632..31068649hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg381018
hg191018
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553096
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261348
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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