A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564748



Internal ID21513055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186464229..186465323hg38UCSC Ensembl
chr3:186182018..186183112hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg381095
hg191095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135283
SamplesNA19983
Known GenesLOC253573
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5564748
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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