A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16290597



Internal ID20499815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:143461782..143461782hg38UCSC Ensembl
chr5:142841347..142841347hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757463
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16290597
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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