A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439709



Internal ID22497579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:115064692..115064692hg38UCSC Ensembl
chr8:116076921..116076921hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5966834
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439709
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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