A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288736



Internal ID20497954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113237862..113237862hg38UCSC Ensembl
chr11:113108584..113108584hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758066
Supporting Variants
Samples
Known GenesNCAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288736
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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