A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185802



Internal ID20752842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94637563..94646733hg38UCSC Ensembl
chr10:96397320..96406490hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg389171
hg199171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6451082
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185802
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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