A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18183942



Internal ID20750982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133559901..133566400hg38UCSC Ensembl
chr10:135373405..135379904hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386500
hg196500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444051
Supporting Variants
Samples
Known GenesSYCE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18183942
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0023


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