A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924142



Internal ID22699369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:125777286..125812756hg38UCSC Ensembl
chr8:126789530..126825000hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3835471
hg1935471
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924142
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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