A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459303



Internal ID21116856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100788267..100794475hg38UCSC Ensembl
chr11:100658998..100665206hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg386209
hg196209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985103
Samples
Known GenesARHGAP42
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459303
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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