A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471225



Internal ID21128778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69237229..69261541hg38UCSC Ensembl
chr11:69004696..69029008hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3824313
hg1924313
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471225
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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