A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5962791



Internal ID22737726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21797272..21797272hg38UCSC Ensembl
chr8:21654784..21654784hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38169
hg19169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17442345
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5962791
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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