A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555444



Internal ID20928531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31303388..31316892hg38UCSC Ensembl
chr22:31699374..31712878hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3813505
hg1913505
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205010
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555444
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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