A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100751



Internal ID21450155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38175673..38175673hg38UCSC Ensembl
chr18:35755637..35755637hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382986
hg192986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658186
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100751
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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