A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489787



Internal ID267058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69280190..69293953hg38UCSC Ensembl
chr10:71039946..71053709hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3813764
hg1913764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035110
Samples
Known GenesHK1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489787
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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