A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5458662



Internal ID236682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47164486..47164793hg38UCSC Ensembl
chr4:47166503..47166810hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16950912
Samples
Known GenesGABRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5458662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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