A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457964



Internal ID21115517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111598901..111606400hg38UCSC Ensembl
chr11:111469625..111477124hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178208
Samples
Known GenesSIK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457964
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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