A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472257



Internal ID21129810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83254462..83273248hg38UCSC Ensembl
chr11:82965504..82984291hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3818787
hg1918788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994047
Samples
Known GenesCCDC90B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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