A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5830618



Internal ID22605553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65551074..65559725hg38UCSC Ensembl
chr1:66016757..66025408hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg388652
hg198652
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17481139
Samples
Known GenesLEPR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5830618
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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