A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4754296



Internal ID20530156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10884126..10884126hg38UCSC Ensembl
chr16:10977983..10977983hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293826
Samples
Known GenesCIITA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4754296
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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