A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191973



Internal ID20759013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114863438..114892059hg38UCSC Ensembl
chr10:116623197..116651818hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3828622
hg1928622
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440483
Supporting Variants
Samples
Known GenesFAM160B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191973
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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