A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626381



Internal ID21574686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159300449..159300449hg38UCSC Ensembl
chr5:158727457..158727457hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17127391
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626381
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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