A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125869



Internal ID21452532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102223115..102223115hg38UCSC Ensembl
chr4:103144272..103144272hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38346
hg19346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616748
Supporting Variants
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125869
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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