A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259677



Internal ID20826717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:136703907..136704325hg38UCSC Ensembl
chr3:136422749..136423167hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568060
Supporting Variants
Samples
Known GenesSTAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259677
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00038


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