A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101112



Internal ID21450635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32855273..32855273hg38UCSC Ensembl
chr18:30435236..30435236hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648004
Supporting Variants
SamplesHG01505
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101112
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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