A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469033



Internal ID21126586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113238962..113244180hg38UCSC Ensembl
chr11:113109684..113114902hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg385219
hg195219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986856
Samples
Known GenesNCAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469033
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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