A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5898994



Internal ID22674119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18119248..18125802hg38UCSC Ensembl
chr4:18120871..18127425hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg386555
hg196555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418657
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5898994
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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