A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215550



Internal ID20782590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130378300..130378631hg38UCSC Ensembl
chr6:130699445..130699776hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618734
Supporting Variants
Samples
Known GenesTMEM200A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215550
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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