A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5565087



Internal ID21513397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39197874..39197933hg38UCSC Ensembl
chr3:39239365..39239424hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138372
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5565087
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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