A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459237



Internal ID21116790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131036503..131371877hg38UCSC Ensembl
chr11:130906398..131241772hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38335375
hg19335375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184841
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459237
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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