A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931689



Internal ID22706976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109486838..109494335hg38UCSC Ensembl
chr13:110139185..110146682hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg387498
hg197498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931689
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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