A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17433327



Internal ID22491197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23522866..23522866hg38UCSC Ensembl
chr8:23380379..23380379hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5952530
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17433327
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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