A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468912



Internal ID21126465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:80374217..80438470hg38UCSC Ensembl
chr11:80085261..80149514hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3864254
hg1964254
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183582
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468912
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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