A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16270769



Internal ID20479987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41488759..41488759hg38UCSC Ensembl
chr11:41510309..41510309hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4759179
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16270769
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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