A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13708519



Internal ID21230308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45080440..45080440hg38UCSC Ensembl
chr22:45476321..45476321hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804822
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13708519
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.703125


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