A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4431168



Internal ID21393170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113752885..113753459hg38UCSC Ensembl
chr10:115512644..115513218hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15747404, nssv15752579
SamplesSMI034, SMI041
Known GenesPLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4431168
Frequency
Sample Size15
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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