A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16261056



Internal ID20470274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51111129..51111129hg38UCSC Ensembl
chr5:50406963..50406963hg19UCSC Ensembl
Cytoband5q11.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750988
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16261056
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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