A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145384



Internal ID21421297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58163288..58163373hg38UCSC Ensembl
chr8:59075847..59075932hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5570091
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145384
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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