A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391698



Internal ID21382728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8923873..8924066hg38UCSC Ensembl
chr17:8827190..8827383hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706111
Samples
Known GenesPIK3R5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391698
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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