A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100816



Internal ID21471363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26433951..26433951hg38UCSC Ensembl
chr18:24013915..24013915hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5652063
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100816
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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