A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467892



Internal ID21125445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129813952..129816355hg38UCSC Ensembl
chr11:129683847..129686250hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382404
hg192404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987739
Samples
Known GenesTMEM45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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