A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585862



Internal ID21534410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101283186..101284938hg38UCSC Ensembl
chr10:103042943..103044695hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381753
hg191753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068451
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585862
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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