A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16268889



Internal ID20478107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6117675..6117787hg38UCSC Ensembl
chr20:6098322..6098434hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732605
Supporting Variants
Samples
Known GenesFERMT1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16268889
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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