A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17544413



Internal ID21868768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77994767..77994767hg38UCSC Ensembl
chr5:77290591..77290591hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17544413
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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