A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600032



Internal ID21548670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102087102..102092459hg38UCSC Ensembl
chr10:103846859..103852216hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385358
hg195358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067468
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600032
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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