A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276379



Internal ID20485597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113781225..113781447hg38UCSC Ensembl
chr10:115540984..115541206hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38223
hg19223
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732874
Supporting Variants
Samples
Known GenesPLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276379
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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