A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460017



Internal ID21117570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99720183..99766826hg38UCSC Ensembl
chr11:99590914..99637557hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3846644
hg1946644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996599
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460017
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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