A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864128



Internal ID22639063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58944318..58946617hg38UCSC Ensembl
chr10:60704078..60706377hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864128
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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