A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441865



Internal ID21099418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26183433..26201004hg38UCSC Ensembl
chr10:26472362..26489933hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3817572
hg1917572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193932
Samples
Known GenesMYO3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441865
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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