A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191034



Internal ID20758074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87836265..87847187hg38UCSC Ensembl
chr10:89596022..89606944hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3810923
hg1910923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6455236
Supporting Variants
Samples
Known GenesCFL1P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191034
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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