A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589074



Internal ID21537638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69297616..69300766hg38UCSC Ensembl
chr10:71057372..71060522hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg383151
hg193151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071147
SamplesHG03065
Known GenesHK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589074
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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