A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804782



Internal ID21250120
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 StatusM
Merged Variants
Supporting Variantsnssv13682379
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804782
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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