A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4389053



Internal ID21380188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87644457..87644507hg38UCSC Ensembl
chr9:90259372..90259422hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15704684
Samples
Known GenesDAPK1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceWong_et_al_2019
Pubmed ID31340865
Accession Number(s)nsv4389053
Frequency
Sample Size174
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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