A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213146



Internal ID20780186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122892392..122926481hg38UCSC Ensembl
chr5:122228087..122262176hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg3834090
hg1934090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6396806
Supporting Variants
Samples
Known GenesSNX24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213146
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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