A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459806



Internal ID21117359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63255101..63257700hg38UCSC Ensembl
chr11:63022573..63025172hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993773
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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