A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452721



Internal ID21110274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92404788..92420416hg38UCSC Ensembl
chr10:94164545..94180173hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3815629
hg1915629
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179466
Samples
Known GenesMARK2P9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452721
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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