A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084710



Internal ID21453472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21177331..21177331hg38UCSC Ensembl
chr16:21188652..21188652hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657888
Supporting Variants
SamplesHG02011
Known GenesTMEM159
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084710
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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