A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490714



Internal ID267965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106876129..106876182hg38UCSC Ensembl
chr7:106516574..106516627hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000935
Samples
Known GenesPIK3CG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490714
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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