A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986089



Internal ID20553129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106675601..106676500hg38UCSC Ensembl
chr11:106546327..106547226hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464462
Supporting Variants
Samples
Known GenesGUCY1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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