A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593858



Internal ID21542449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:38073377..38073683hg38UCSC Ensembl
chr10:38362305..38362611hg19UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070195
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593858
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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