A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460451



Internal ID21118004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72432676..72446662hg38UCSC Ensembl
chr11:72143720..72157706hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3813987
hg1913987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193785
Samples
Known GenesCLPB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460451
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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