A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158219



Internal ID21494045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42585754..42585805hg38UCSC Ensembl
chr8:42440897..42440948hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581556
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158219
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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