A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17150341



Internal ID21463820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:135948598..135948793hg38UCSC Ensembl
chr8:136960841..136961036hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566069
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17150341
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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