A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844879



Internal ID22619814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35365132..35366731hg38UCSC Ensembl
chr6:35332909..35334508hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17505338
Samples
Known GenesPPARD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844879
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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