A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638325



Internal ID21586630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25088857..25088857hg38UCSC Ensembl
chr5:25088966..25088966hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124029
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638325
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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