A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907650



Internal ID5881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:111158903..111159213hg38UCSC Ensembl
chr1:111701525..111701835hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423282
Supporting Variants
Samples
Known GenesCEPT1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907650
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.008898


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