A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4392453



Internal ID21383483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5339129..5346309hg38UCSC Ensembl
chr20:5319775..5326955hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg387181
hg197181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15706484
Samples
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4392453
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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