A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144389



Internal ID21456912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116442124..116442124hg38UCSC Ensembl
chr8:117454362..117454362hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg381995
hg191995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631677
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144389
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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