A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5950984



Internal ID22726373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133970655..133970655hg38UCSC Ensembl
chr8:134982898..134982898hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17437523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5950984
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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