A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095615



Internal ID21466284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30905132..30913355hg38UCSC Ensembl
chr16:30916453..30924676hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg388224
hg198224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604393
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095615
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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