A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894237



Internal ID22669308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:611332..611601hg38UCSC Ensembl
chr4:605121..605390hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17425579
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894237
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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