A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140768



Internal ID21509366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104074791..104075218hg38UCSC Ensembl
chr8:105087019..105087446hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570936
Supporting Variants
SamplesNA20847
Known GenesRIMS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140768
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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