A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937752



Internal ID22713124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:101997193..101997302hg38UCSC Ensembl
chr13:102649543..102649652hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365189
Samples
Known GenesFGF14
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937752
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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