A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682379



Internal ID21204237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36126545..36126545hg38UCSC Ensembl
chr22:36522593..36522593hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38526
hg19526
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804782
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682379
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.323529


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