A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101828



Internal ID21488281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55018506..55021435hg38UCSC Ensembl
chr18:52685737..52688666hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg382930
hg192930
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602197
Supporting Variants
SamplesNA18939
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101828
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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