A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262332



Internal ID20471550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53426432..53426432hg38UCSC Ensembl
chr5:52722262..52722262hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262332
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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