A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553670



Internal ID20926781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:30698542..30705488hg38UCSC Ensembl
chr22:31094529..31101475hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg386947
hg196947
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204998
Samples
Known GenesOSBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553670
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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