A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445866



Internal ID21103419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124784784..124793651hg38UCSC Ensembl
chr10:126473353..126482220hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg388868
hg198868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978027
Samples
Known GenesMETTL10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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