A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067779



Internal ID21404109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131986695..131986767hg38UCSC Ensembl
chr10:133800199..133800271hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5585220
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067779
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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