A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15747404



Internal ID21392903
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 StatusS
Merged Variantsnsv4431168
Supporting Variants
SamplesSMI041
Known GenesPLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15747404
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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