A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446375



Internal ID21103928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89062370..89071323hg38UCSC Ensembl
chr10:90822127..90831080hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg388954
hg198954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17984926
Samples
Known GenesMIR4679-1, MIR4679-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446375
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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