A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464848



Internal ID21122401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83269495..83271656hg38UCSC Ensembl
chr11:82980537..82982698hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382162
hg192162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994048
Samples
Known GenesCCDC90B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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