A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435744



Internal ID22493614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108657860..108657860hg38UCSC Ensembl
chr8:109670089..109670089hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950845
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435744
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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