A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486706



Internal ID264064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102313196..102313637hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38442
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000193
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486706
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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