A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628163



Internal ID21576468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62864440..62864440hg38UCSC Ensembl
chr10:64624200..64624200hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070457
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628163
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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