A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589112



Internal ID21537676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102911024..102911074hg38UCSC Ensembl
chr10:104670781..104670831hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068464
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589112
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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