A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4391087



Internal ID21379666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26202185..26202580hg38UCSC Ensembl
chr4:26203807..26204202hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15703022
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4391087
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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