A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17091317



Internal ID21469873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11817233..11817721hg38UCSC Ensembl
chr16:11911090..11911578hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38489
hg19489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5594487
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17091317
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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