A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4388793



Internal ID21379928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39950984..39951378hg38UCSC Ensembl
chr8:39808503..39808897hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38395
hg19395
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704395
Samples
Known GenesIDO2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4388793
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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