A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460046



Internal ID21117599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98952049..99008493hg38UCSC Ensembl
chr11:98822779..98879223hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3856445
hg1956445
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996502
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460046
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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