A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5629831



Internal ID21578136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130013972..130013972hg38UCSC Ensembl
chr10:131812236..131812236hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066835
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5629831
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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