A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143142



Internal ID21488200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:100445955..100446037hg38UCSC Ensembl
chr8:101458183..101458265hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571378
Supporting Variants
SamplesNA18534
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143142
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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