A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553309



Internal ID20926418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43153019..43181623hg38UCSC Ensembl
chr22:43549025..43577629hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3828605
hg1928605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207529
Samples
Known GenesTSPO, TTLL12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553309
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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