A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086210



Internal ID21453039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19489000..19489054hg38UCSC Ensembl
chr16:19500322..19500376hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595915
Supporting Variants
SamplesHG02011
Known GenesTMC5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086210
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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