A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230736



Internal ID20797776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57707276..57707814hg38UCSC Ensembl
chr11:57474748..57475286hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591410
Supporting Variants
Samples
Known GenesMED19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230736
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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