A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471775



Internal ID21129328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:99276209..99341474hg38UCSC Ensembl
chr11:99146940..99212205hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3865266
hg1965266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178561
Samples
Known GenesCNTN5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471775
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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