A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458772



Internal ID236793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148087993..148107065hg38UCSC Ensembl
chr4:149009144..149028216hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3819073
hg1919073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16956982
Samples
Known GenesNR3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458772
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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