A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6457071



Internal ID21114624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66649201..66650957hg38UCSC Ensembl
chr11:66416672..66418428hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381757
hg191757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992581
Samples
Known GenesRBM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6457071
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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