A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083998



Internal ID21512047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88313992..88314165hg38UCSC Ensembl
chr16:88347598..88347771hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5590859
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083998
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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