A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469335



Internal ID21126888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61941622..61942273hg38UCSC Ensembl
chr11:61709094..61709745hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38652
hg19652
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188336
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469335
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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