A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204632



Internal ID20771672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37556154..37577412hg38UCSC Ensembl
chr22:37952161..37973419hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3821259
hg1921259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544785
Supporting Variants
Samples
Known GenesCDC42EP1, LGALS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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