A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469475



Internal ID21127028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128183482..128198338hg38UCSC Ensembl
chr11:128053377..128068233hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3814857
hg1914857
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469475
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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