A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5892277



Internal ID22667325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:89122221..89122533hg38UCSC Ensembl
chr4:90043372..90043684hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5892277
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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