A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5841484



Internal ID22616419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149847720..149871893hg38UCSC Ensembl
chr5:149227283..149251456hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3824174
hg1924174
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17496271
Samples
Known GenesPDE6A, PPARGC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5841484
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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