A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986756



Internal ID20553796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:111367282..111372319hg38UCSC Ensembl
chr11:111238007..111243044hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg385038
hg195038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460827
Supporting Variants
Samples
Known GenesPOU2AF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986756
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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