A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444233



Internal ID21101786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62227471..62227883hg38UCSC Ensembl
chr10:63987230..63987642hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982633
Samples
Known GenesRTKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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