A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152156



Internal ID21468229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93936689..93936823hg38UCSC Ensembl
chr8:94948917..94949051hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5581643
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152156
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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