A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392183



Internal ID21383213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:153287700..153288147hg38UCSC Ensembl
chr5:152667260..152667707hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703629
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392183
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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