A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466273



Internal ID244116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6456839..6457433hg38UCSC Ensembl
chr7:6496470..6497064hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16991627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466273
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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