A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448876



Internal ID21106429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67023378..67100130hg38UCSC Ensembl
chr10:68783136..68859888hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3876753
hg1976753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189875
Samples
Known GenesCTNNA3, LRRTM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448876
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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