A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638948



Internal ID21587253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101699439..101699439hg38UCSC Ensembl
chr10:103459196..103459196hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3819450
hg1919450
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067455
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638948
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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