A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181902



Internal ID20748942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91929909..92166613hg38UCSC Ensembl
chr10:93689666..93926370hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38236705
hg19236705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453021
Supporting Variants
Samples
Known GenesBTAF1, CPEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181902
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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