A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468255



Internal ID21125808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82560805..82611853hg38UCSC Ensembl
chr11:82271847..82322895hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3851049
hg1951049
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468255
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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