A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099993



Internal ID21467138
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 StatusS
Merged Variantsnsv5585720
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099993
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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