A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5488281



Internal ID265600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106175564..106179811hg38UCSC Ensembl
chr7:105816010..105820257hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg384248
hg194248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000890
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5488281
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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