A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431142



Internal ID22489012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:27593393..27593393hg38UCSC Ensembl
chr8:27450910..27450910hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957553
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431142
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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