A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206834



Internal ID20773875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:41946385..41954121hg38UCSC Ensembl
chr22:42342389..42350125hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg387737
hg197737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553416
Supporting Variants
Samples
Known GenesCENPM, LINC00634
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206834
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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