A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903642



Internal ID22678811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8376085..8446431hg38UCSC Ensembl
chr4:8377812..8448158hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3870347
hg1970347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17417068
Samples
Known GenesACOX3, TRMT44
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903642
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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