A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280005



Internal ID20489223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63615027..63615027hg38UCSC Ensembl
chr11:63382499..63382499hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760239
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280005
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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