A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458226



Internal ID21115779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85929192..85974323hg38UCSC Ensembl
chr11:85640235..85685366hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3845132
hg1945132
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192638
Samples
Known GenesPICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458226
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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