A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5575387



Internal ID21523816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:117910387..117910598hg38UCSC Ensembl
chr3:117629234..117629445hg19UCSC Ensembl
Cytoband3q13.32
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132242
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5575387
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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