A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151069



Internal ID21457050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37946064..37946361hg38UCSC Ensembl
chr8:37803582..37803879hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5583387
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151069
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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