A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449058



Internal ID21106611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104960985..105815666hg38UCSC Ensembl
chr10:106720743..107575424hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38854682
hg19854682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185883
Samples
Known GenesSORCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449058
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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