A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444066



Internal ID21101619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49745181..49747187hg38UCSC Ensembl
chr10:50953227..50955233hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382007
hg192007
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17981848
Samples
Known GenesOGDHL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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