A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501089



Internal ID278000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70228323..70237592hg38UCSC Ensembl
chr11:70074429..70083698hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg389270
hg199270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046415
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501089
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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