A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225675



Internal ID20792715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40055658..40058900hg38UCSC Ensembl
chr11:40077208..40080450hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg383243
hg193243
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6580000
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225675
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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