A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219793



Internal ID20786833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17280756..17281389hg38UCSC Ensembl
chr11:17302303..17302936hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38634
hg19634
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585572
Supporting Variants
Samples
Known GenesNUCB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219793
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0005


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