A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899274



Internal ID22674402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182655351..182659374hg38UCSC Ensembl
chr4:183576504..183580527hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg384024
hg194024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422959
Samples
Known GenesTENM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899274
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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