A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931381



Internal ID22706664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24738266..24738326hg38UCSC Ensembl
chr16:24749587..24749647hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370785
Samples
Known GenesTNRC6A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931381
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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