A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465129



Internal ID21122682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129745609..129826276hg38UCSC Ensembl
chr11:129615504..129696171hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3880668
hg1980668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988154
Samples
Known GenesTMEM45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465129
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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