A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641802



Internal ID21590107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87533677..87533677hg38UCSC Ensembl
chr5:86829494..86829494hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17149855
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641802
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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