A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204643



Internal ID20771683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38040606..38068404hg38UCSC Ensembl
chr22:38436613..38464411hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3827799
hg1927799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539874
Supporting Variants
Samples
Known GenesPICK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204643
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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