A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564685



Internal ID21512991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68127780..68127872hg38UCSC Ensembl
chr3:68176930..68177022hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17134250
SamplesHG03065
Known GenesFAM19A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5564685
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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