A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468176



Internal ID21125729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69487321..69530633hg38UCSC Ensembl
chr11:69302089..69345401hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3843313
hg1943313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17992707
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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