A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17128065



Internal ID21442345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10866..10866hg38UCSC Ensembl
chr4:10866..10866hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38232
hg19232
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5617451
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17128065
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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