A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235242



Internal ID20802282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9237953..9238404hg38UCSC Ensembl
chr11:9259500..9259951hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6585515
Supporting Variants
Samples
Known GenesDENND5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235242
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00021


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