A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804781



Internal ID21250119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36126524..36126524hg38UCSC Ensembl
chr22:36522572..36522572hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678282
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804781
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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