A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411886



Internal ID22469756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:67486952..67486952hg38UCSC Ensembl
chr5:66782780..66782780hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5956439
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411886
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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