A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566337



Internal ID21514662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148183016..148183092hg38UCSC Ensembl
chr3:147900803..147900879hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137795
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566337
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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