A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441469



Internal ID21099022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20457121..20562967hg38UCSC Ensembl
chr10:20746050..20851896hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38105847
hg19105847
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186001
Samples
Known GenesMIR4675
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441469
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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