A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474031



Internal ID21131584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129850264..129862163hg38UCSC Ensembl
chr11:129720159..129732058hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987746
Samples
Known GenesTMEM45B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474031
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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