A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435430



Internal ID22493300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103451125..103451125hg38UCSC Ensembl
chr8:104463353..104463353hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435430
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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