A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459565



Internal ID21117118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118561877..118562454hg38UCSC Ensembl
chr11:118432592..118433169hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38578
hg19578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986614
Samples
Known GenesIFT46
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459565
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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