A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442379



Internal ID21099932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3161697..3163591hg38UCSC Ensembl
chr11:3182927..3184821hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381895
hg191895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989686
Samples
Known GenesOSBPL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442379
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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