A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445813



Internal ID21103366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55239401..55519900hg38UCSC Ensembl
chr10:56999161..57279660hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38280500
hg19280500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv751n223
Supporting Variantsnssv18181884
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445813
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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