A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472686



Internal ID21130239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118823256..118828030hg38UCSC Ensembl
chr11:118693965..118698739hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384775
hg194775
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986629
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472686
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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