A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2804440



Internal ID21249778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:34034610..34034610hg38UCSC Ensembl
chr22:34430599..34430599hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13678406, nssv13687689
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2804440
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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