A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986101



Internal ID20553141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106750747..106755151hg38UCSC Ensembl
chr11:106621473..106625877hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg384405
hg194405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457213
Supporting Variants
Samples
Known GenesGUCY1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986101
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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