A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466055



Internal ID21123608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93188007..93188493hg38UCSC Ensembl
chr11:92921173..92921659hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996455
Samples
Known GenesSLC36A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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