A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392092



Internal ID21383122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:124832150..124841311hg38UCSC Ensembl
chr5:124167843..124177004hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg389162
hg199162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703583
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392092
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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