A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234100



Internal ID20801140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:30898121..30900005hg38UCSC Ensembl
chr11:30919668..30921552hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg381885
hg191885
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586698
Supporting Variants
Samples
Known GenesDCDC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234100
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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