A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567660



Internal ID21515998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141771409..141771493hg38UCSC Ensembl
chr3:141490251..141490335hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132328
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567660
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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