A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17144390



Internal ID21438707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45904647..45904647hg38UCSC Ensembl
chr6:45872384..45872384hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624859
Supporting Variants
SamplesHG00732
Known GenesCLIC5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17144390
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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