A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152827



Internal ID21475821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69204051..69204051hg38UCSC Ensembl
chr5:68499878..68499878hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634625
Supporting Variants
SamplesHG03486
Known GenesCENPH
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152827
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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