A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5585720



Internal ID21534268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11681641..11686419hg38UCSC Ensembl
chr18:11681640..11686418hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg384779
hg194779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099993
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5585720
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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