A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17155146



Internal ID21494510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91699961..91700285hg38UCSC Ensembl
chr8:92712189..92712513hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583514
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17155146
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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