A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890094



Internal ID22665119
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 Variantsnssv17443273
Samples
Known GenesPPARD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890094
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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