A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460253



Internal ID21117806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:133771659..133796375hg38UCSC Ensembl
chr11:133641554..133666270hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3824717
hg1924717
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185737
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460253
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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