A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465446



Internal ID21122999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61340198..61351445hg38UCSC Ensembl
chr11:61107670..61118917hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3811248
hg1911248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993136
Samples
Known GenesCYB561A3, DAK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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