A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907886



Internal ID22683096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40224300..40226921hg38UCSC Ensembl
chr8:40081819..40084440hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg382622
hg192622
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907886
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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