A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216213



Internal ID20783253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:33513987..33514540hg38UCSC Ensembl
chr5:33514092..33514645hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6376875
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216213
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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