A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639929



Internal ID21588234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80592..80592hg38UCSC Ensembl
chr10:126532..126532hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38503
hg19503
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071345
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639929
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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