A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17140587



Internal ID21412489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128328849..128328928hg38UCSC Ensembl
chr8:129341095..129341174hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5565734
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17140587
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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