A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5928778



Internal ID22704022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68864576..68917868hg38UCSC Ensembl
chr13:69438708..69492000hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3853293
hg1953293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17385845
Samples
Known GenesLINC00550
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5928778
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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