A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5567434



Internal ID21515770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:178062355..178063599hg38UCSC Ensembl
chr3:177780143..177781387hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124263
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5567434
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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