A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218308



Internal ID20785348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3964771..3966001hg38UCSC Ensembl
chr11:3986001..3987231hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381231
hg191231
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582237
Supporting Variants
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218308
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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