A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17154751



Internal ID21505842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132510317..132510317hg38UCSC Ensembl
chr8:133522564..133522564hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5636904
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17154751
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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