A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088500



Internal ID21412414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60047208..60064656hg38UCSC Ensembl
chr16:60081112..60098560hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3817449
hg1917449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601215
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088500
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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