A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261331



Internal ID20470549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9082997..9082997hg38UCSC Ensembl
chr11:9104544..9104544hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg382147
hg192147
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756431
Supporting Variants
Samples
Known GenesSCUBE2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261331
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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