A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457328



Internal ID21114881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87768508..87825583hg38UCSC Ensembl
chr11:87479400..87536475hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3857076
hg1957076
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457328
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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