A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938953



Internal ID22714340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89875732..89878878hg38UCSC Ensembl
chr16:89942140..89945286hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg383147
hg193147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379859
Samples
Known GenesTCF25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938953
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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