A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182566



Internal ID20749606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92551866..92561512hg38UCSC Ensembl
chr10:94311623..94321269hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg389647
hg199647
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446002
Supporting Variants
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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