A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480970



Internal ID258466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66098062..66099872hg38UCSC Ensembl
chr7:65563049..65564859hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381811
hg191811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16997618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480970
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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