A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5905681



Internal ID22680871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69799515..69799564hg38UCSC Ensembl
chr4:70665233..70665282hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5905681
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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