A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681838



Internal ID21203699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33132513..33132513hg38UCSC Ensembl
chr22:33528499..33528499hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804630
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681838
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.296875


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