A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5829759



Internal ID22604694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:243106184..243153716hg38UCSC Ensembl
chr1:243269486..243317018hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3847533
hg1947533
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464929
Samples
Known GenesCEP170
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5829759
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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