A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684762



Internal ID21206619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44863121..44863121hg38UCSC Ensembl
chr21:46283036..46283036hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803682
Supporting Variants
Samples
Known GenesPTTG1IP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684762
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.152174


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