A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449606



Internal ID22507476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116780544..116780544hg38UCSC Ensembl
chr8:117792783..117792783hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449606
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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