A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5635828



Internal ID21584133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6242593..6242593hg38UCSC Ensembl
chr10:6284556..6284556hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070450
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5635828
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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