A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205679



Internal ID20772719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48870950..48887794hg38UCSC Ensembl
chr22:49266762..49283606hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3816845
hg1916845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547866
Supporting Variants
Samples
Known GenesLOC100128946
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205679
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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