A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450726



Internal ID21108279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88936714..89008323hg38UCSC Ensembl
chr10:90696471..90768080hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3871610
hg1971610
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177450
Samples
Known GenesACTA2, FAS, FAS-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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