A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863728



Internal ID22638663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99609250..99618240hg38UCSC Ensembl
chr13:100261504..100270494hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg388991
hg198991
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460085
Samples
Known GenesCLYBL
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863728
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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