A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678322



Internal ID21200178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219159514..219159514hg38UCSC Ensembl
chr2:220024236..220024236hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807147
Supporting Variants
Samples
Known GenesNHEJ1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678322
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.421875


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