A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213286



Internal ID20780326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150374196..150438419hg38UCSC Ensembl
chr5:149753759..149817982hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3864224
hg1964224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414572
Supporting Variants
Samples
Known GenesCD74, TCOF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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