A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951190



Internal ID22726564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:102541898..102541898hg38UCSC Ensembl
chr8:103554126..103554126hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951190
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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