A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938166



Internal ID22713544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:69262147..69285422hg38UCSC Ensembl
chr13:69836279..69859554hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3823276
hg1923276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372511
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938166
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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