A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5459851



Internal ID237857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:22215002..22215846hg38UCSC Ensembl
chr7:22254621..22255465hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16993878
Samples
Known GenesRAPGEF5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5459851
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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