A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463490



Internal ID21121043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119878896..119917393hg38UCSC Ensembl
chr11:119749605..119788102hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3838498
hg1938498
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463490
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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