A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5578581



Internal ID21527052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106111642..106111718hg38UCSC Ensembl
chr3:105830489..105830565hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17129417
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5578581
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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