A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639669



Internal ID21587974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:25822719..25822719hg38UCSC Ensembl
chr10:26111648..26111648hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17069765
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639669
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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