A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581819



Internal ID21530323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122363277..122363873hg38UCSC Ensembl
chr3:122082124..122082720hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17138704
SamplesHG03486
Known GenesCCDC58
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581819
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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