A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182074



Internal ID20749114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100909001..100916900hg38UCSC Ensembl
chr10:102668758..102676657hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436536
Supporting Variants
Samples
Known GenesFAM178A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182074
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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