A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467088



Internal ID21124641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62366637..62385395hg38UCSC Ensembl
chr11:62134109..62152867hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3818759
hg1918759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1205n223
Supporting Variantsnssv18195910
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467088
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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