A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469042



Internal ID21126595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99412579..99544123hg38UCSC Ensembl
chr11:99283310..99414854hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38131545
hg19131545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996559
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469042
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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