A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471442



Internal ID21128995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126286193..126288376hg38UCSC Ensembl
chr11:126156088..126158271hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg382184
hg192184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987332
Samples
Known GenesTIRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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