A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585085



Internal ID21533630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64509026..64509334hg38UCSC Ensembl
chr10:66268783..66269091hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071234
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585085
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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