A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626333



Internal ID21574638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8260597..8260597hg38UCSC Ensembl
chr5:8260710..8260710hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150043
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626333
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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