A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450365



Internal ID21107918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62204132..62204668hg38UCSC Ensembl
chr10:63963891..63964427hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982628
Samples
Known GenesRTKN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450365
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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