A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036203



Internal ID21945546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68817812..68832286hg38UCSC Ensembl
chr11:68585280..68599754hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3814475
hg1914475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584180
Samples
Known GenesCPT1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036203
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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