A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463543



Internal ID22521429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68816592..68826598hg38UCSC Ensembl
chr11:68584060..68594066hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3810007
hg1910007
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5854581
Supporting Variants
Samples
Known GenesCPT1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463543
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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