A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100587



Internal ID21444403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11959580..11959695hg38UCSC Ensembl
chr18:11959579..11959694hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593407
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100587
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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