A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633653



Internal ID21581958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4576725..4576725hg38UCSC Ensembl
chr10:4618917..4618917hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070529
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633653
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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