A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449160



Internal ID21106713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48346830..48367981hg38UCSC Ensembl
chr10:49554873..49576024hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3821152
hg1921152
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195161
Samples
Known GenesMAPK8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449160
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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