A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103788



Internal ID21450161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:8750086..8750086hg38UCSC Ensembl
chr18:8750084..8750084hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655015
Supporting Variants
SamplesHG01114
Known GenesSOGA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103788
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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