A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455866



Internal ID21113419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121202241..121214332hg38UCSC Ensembl
chr11:121072950..121085041hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3812092
hg1912092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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