A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5965456



Internal ID22740391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28684945..28684945hg38UCSC Ensembl
chr8:28542462..28542462hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17430534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5965456
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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