A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5455190



Internal ID233272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4728194..4731260hg38UCSC Ensembl
chr7:4767825..4770891hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg383067
hg193067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16992473
Samples
Known GenesFOXK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5455190
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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