A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890508



Internal ID22665536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:113892211..113892534hg38UCSC Ensembl
chr4:114813367..114813690hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415085
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890508
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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