A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986105



Internal ID20553145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106789470..106801108hg38UCSC Ensembl
chr11:106660196..106671834hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3811639
hg1911639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475535
Supporting Variants
Samples
Known GenesGUCY1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986105
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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