A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566062



Internal ID21514381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67593226..67593353hg38UCSC Ensembl
chr3:67643650..67643777hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17124711
SamplesNA19238
Known GenesSUCLG2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566062
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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