A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5568289



Internal ID21516635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66712829..66712885hg38UCSC Ensembl
chr3:66763253..66763309hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132489
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5568289
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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