A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151853



Internal ID21503544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:29667128..29667128hg38UCSC Ensembl
chr8:29524644..29524644hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38238
hg19238
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634083
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151853
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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