A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442648



Internal ID21100201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:17060770..17072114hg38UCSC Ensembl
chr11:17082317..17093661hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811345
hg1911345
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189966
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442648
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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