A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467237



Internal ID21124790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106259284..106278149hg38UCSC Ensembl
chr11:106130011..106148876hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3818866
hg1918866
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467237
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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