A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864169



Internal ID22639104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:50004558..50006969hg38UCSC Ensembl
chr13:50578694..50581105hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg382412
hg192412
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456361
Samples
Known GenesDLEU2, TRIM13
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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