A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643998



Internal ID21592303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4815475..4815475hg38UCSC Ensembl
chr10:4857667..4857667hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070591
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643998
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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