A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5566807



Internal ID21515136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35425222..35425356hg38UCSC Ensembl
chr6:35392999..35393133hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17144253
SamplesHG00096
Known GenesPPARD
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5566807
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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