A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857048



Internal ID22631983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68876151..68878750hg38UCSC Ensembl
chr13:69450283..69452882hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451810, nssv17467611
Samples
Known GenesLINC00550
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857048
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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