A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17159466



Internal ID21479051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96057676..96057727hg38UCSC Ensembl
chr8:97069904..97069955hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5568382
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17159466
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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