A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16288449



Internal ID20497667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67339328..67339328hg38UCSC Ensembl
chr5:66635156..66635156hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4766955
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16288449
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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