A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5482126



Internal ID259586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145479199..145529444hg38UCSC Ensembl
chr7:145176292..145226537hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3850246
hg1950246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17004581
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5482126
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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