A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5859981



Internal ID22634916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103000282..103001281hg38UCSC Ensembl
chr7:102640729..102641728hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500081
Samples
Known GenesFBXL13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5859981
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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