A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450784



Internal ID21108337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18554739..18555144hg38UCSC Ensembl
chr10:18843668..18844073hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190228
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450784
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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